K-Bar List Jobs: 8 Apr 2016
Reminder: The jobs listed below are located on the blog: www.kbarlist.blogspot.com
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Today’s Posting:
1. GC Applications Chemist – Folsom, CA
2. Global Communications Manager – Santa Clara, CA
3. Global Engagements & Enterprise Consulting Manager – Santa Clara, CA
4. Global Media Performance Manager – Englewood, CO
5. Life Science/ Chemical Analysis – Melville, New York
6. Life Science/ Chemical Analysis – Cambridge, MA
7. Multivendor Services Program Manager – Santa Clara, CA
8. Global Compliance Services Program Manager – Santa Clara, CA
9. Project Manager/Data Analyst – Business Analytics – Wilmington, DE
10. Service Business Manager - Puerto Rico
11. QQQ LC/MS Lead Instructor – Lexington, MA
12. R&D Materials Scientist – Santa Clara, CA
13. Researcher - R&D Thin Films – Santa Clara, CA
14. Senior Level Quality Assurance Engineer - Chemistries and Supplies – Folsom, CA
15. Senior Service Engineer- LCMS – Boston, MA
16. Senior Service Engineer- LCMS – Boston, MA
17. Services Product Manager – Santa Clara, CA
18. Software Application Specialist – Carpinteria, CA
19. Technical Support Specialist – Carpinteria, CA
20. OF & Supply Chain Associate Scientist- Cedar Creek, TX
21. OF & Supply Chain Commodity Manager – Wilmington, DE
22. OF & Supply Chain Commodity Manager – Wilmington, DE
23. OF & Supply Chain Engineering Intern – Wilmington, DE
24. OF & Supply Chain Manufacturing Chemist – Newport, DE
25. OF & Supply Chain Manufacturing Operator – Santa Clara, CA
26. OF & Supply Chain Manufacturing Software Implementation Engineer – Wilmington, DE
27. OF & Supply Chain Manufacturing Test Tech – Wilmington, DE
28. OF & Supply Chain Materials Procurement Associate – Sacramento, CA
29. OF & Supply Chain NPI Engineer – Lexington, MA
30. OF & Supply Chain Production Operator – Folsom, CA
31. OF & Supply Chain Shipping Operator – Newport, DE
32. Account Manager- Genomics (Alpharetta, GA)
33. Analytical Services Scientist – Boulder, CO
34. Clinical Affairs Scientist – Carpinteria, CA
35. Clinical Affairs Specialist – Carpinteria, CA
36. Design Control Manager Research Associate – Carpinteria, CA
37. Design Control Specialist Research Associate – Carpinteria, CA
38. Field Applications Scientist - Genomics Automation (Baltimore, MD)
39. Immuno-Histo Chemistry Applications Specialist – Santa Clara, CA
40. Chemist – Boulder, CO
41. Materials Coordinator – Boulder, CO
42. Product Manager- Cytogenetics – Santa Clara, CA
43. Product Manager, Synthetic Biology Products – Santa Clara, CA
44. Project Manager, Companion Diagnostics – Carpinteria, CA
45. Project Manager, Companion Diagnostics – Carpinteria, CA
46. Quality Engineer - New Product Introductions – Santa Clara, CA
47. Regulatory Affairs Specialist – Carpinteria, CA
48. Research Assistant, Companion Diagnostics – Carpinteria, CA
49. Research Assistant, Companion Diagnostics – Carpinteria, CA
50. Research Associate- Histologist – Carpinteria, CA
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1. GC Applications Chemist – Folsom, CA
Req ID: 2065429 Locations: Folsom,California,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group GC Applications Chemist Here is your opportunity to join a high performance consumables marketing team in Agilent’s Chemistries and Supplies Division (CSD). This team is bringing new products and breakthrough marketing approaches into the global market faster and more efficiently than ever before. If you have a passion for delivering strong and profitable growth and have demonstrated customer-centricity, we would be delighted to have you on the Supplies Product Marketing team within CSD. We are seeking an experienced Applications Chemist to develop compelling GC Columns and Supplies applications and technical marketing material in written and oral presentations to drive customer adoption of our products. The successful candidate will focus on developing applications for a variety of gas chromatography related columns and supplies in our global markets including Environmental Testing, Food Safety Testing, Hydrocarbon Processing and Forensics market segments. This position requires a high degree of creativity, teamwork, initiative, self-direction and ability to multi-task to deliver to project deadlines and reports directly to the Senior Marketing Director of the Supplies Division. The candidate will be responsible for the following: Generating new applications, technical data, and proof of performance for a wide range of gas chromatography columns and supplies that address customer needs in target segments. Maintaining updated understanding of the gas chromatography markets and competitive environment. Understanding customer segment needs as a basis to develop new applications and feedback for new product development. Developing content that articulates compelling customer value. Creating market-focused application collateral, i.e. application briefs, compendiums, peer-reviewed articles and posters. Helping with developing user requirement specs for new GC columns and supplies products. Developing a “story” that showcases a compelling customer value proposition for chromatography supplies including economic value. This includes data analysis and presentation in a format that clearly highlights the product’s workflow benefits to users and customers. Conducting lab work to test business relevance of applications as needed. Creating compelling business value content for customers, i.e. sales presentations, competitor performance comparisons, case studies, and white papers Developing and delivering seminars, e-seminars, applications training and key data for marketing collateral Managing and participating in collaborations with key customers and thought leaders in Chemical Analysis, Environmental, Forensics, Food Safety, and other relevant industries to identify application and segment needs, as well as, some or all of the content for applications. Writing technical briefs, application notes and other technical marketing material in a clear and compelling fashion. Ensuring that the final written material is completed and available for use by specified deadlines.
Playing a key role in developing and delivering applications training to sales channels. Providing in person technical expertise at select customers events and conferences, e.g. delivering seminars, giving technical posters Representing Agilent Technologies in the scientific and professional community. Qualifications PhD or Master’s Degree with equivalent experience in Analytical Chemistry, Chemistry or similar discipline Minimum of 5 years of experience in GC or GC/MS applications development or technical marketing. Minimum of 2 years of experience working with tandem MS applications Demonstrated experience and results in technical marketing and/or applications material development in the laboratory. Experience in the analytical laboratory setting as a foundation for understanding customer needs and the channels that serve these customers. Latest experience must be laboratory-based experience developing technical marketing material. Strong GC, GC/MS, and GC/MS/MS experience. Deep understanding of sample prep needs in market segments listed above. Ability to evaluate newly developed products or new breakthrough technologies in gas chromatography. Ability to identify business drivers and communicate value propositions in a business oriented manner An unwavering passion for serving our customer’s needs. Initiative to drive assignments and deliver results on time with a ‘can-do’ attitude Excellent collaboration skills and ability to work in partnership with colleagues within and across organizations as well as with external partners and customers. Excellent oral, written and communication skills. Additional language skills are a plus. Excellent presentation and training skills Experience with writing scientific and business focused documentation Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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2. Global Communications Manager – Santa Clara, CA
Req ID: 2065767 Locations: Santa Clara,California,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Global Communications Manager, Life Sciences and Applied Markets Group Agilent Technologies is a leader in the life sciences and analytical businesses, and growing in diagnostics and genomics markets. The company offers a wide range of scientific instruments, software, consumables and services to create solutions that address some of the world's most pressing challenges. Agilent is #1 or #2 in such dynamic markets as environment, energy and chemical, food and pharma. Our mission is to inspire discoveries that advance the quality of life--and that means we are helping our customers find ways to clean up air and water pollution, ensure purer and safer food; fight cancer and other diseases. Our teams include some of the best scientists and engineers in the world. And our style is collaborative. No matter what your job is, you will find a passion for what we do because we know we are making a difference in helping create a better world. Working directly with the Life Sciences and Applied Markets Group (LSAG) president as part of his leadership team, you are responsible for creating and driving compelling communications to support LSAG's strategic priorities. You will serve as a counselor to the President and colleagues looking to energize their global teams around business initiatives. You will identify and measure effectiveness of communications channels and methods of communication, including innovative new ways of building employee understanding. You will be expected to maintain excellent active relationships with communicators in other leading companies to be able to learn from best practices and apply them as appropriate. This position will assist leadership team in identifying key opportunities to tell the Agilent story internally and externally with a focus on employee communications. Your work on external messaging will be from a broader Agilent perspective, coordinating closely with the PR manager. You will play an important role in implementing M&A messaging in concert with corporate communications teams. The job requires a broad range of communications, project management and people-relationship skills; exceptional proactive internal service skills; the ability to be strategic, but also execute; exceptional writing matched to the "voice" of the LSAG president and other leaders and ability to distill complex messaging into simple, clear messaging. The job also requires a candidate who is tech savvy and able to advise about and implement communications plans that include a wide range of technology-based channels. You must be comfortable operating effectively and diplomatically within a fast-paced organization. The ideal candidate will be a strategist, innovator and excellent storyteller, and will have a positive, can-do attitude, bringing new ideas and innovative approaches to the group. He or she will be expected to deliver results through others who do not report to him/her. Qualifications * Minimum 8 years of demonstrated results in a global communications position * Strong project management skills and ability to execute with speed, accuracy and efficiency * Outstanding influencing and interpersonal skills with a track record of forming effective peer-level relationships with senior members of an organization * Exceptional writing skills, ability to write in different styles to reflect channel, sender's voice, audience and message. *Experience with current web practices, supporting technologies, new media (including viral messaging, social media) *Uncompromising commitment to quality. Detail oriented, but able to see the big picture *Self-motivated with an appetite to work entrepreneurially; track record as a self-starter *Team orientation with strong sense of commitment to team members and internal customers *Flexibility to travel globally as required and to work, if needed, outside of standard office hours. *Minimum Bachelor's Degree *Experience in life sciences a strong plus *Previous experience in a biosciences company is desirable. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for
employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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3. Global Engagements & Enterprise Consulting Manager – Santa Clara, CA
Req ID: 2065496 Locations: Santa Clara,California,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Global Engagements & Enterprise Consulting Manager Laboratory Enterprise Division As the LED Global Engagements & Enterprise Consulting Manager, you are the global business lead for Cross-lab services Enterprise programs, accounts and consulting services. You focus on 2 broad areas of responsibility: • For the global engagements, accounts and programs, you are responsible for all facets of assigned clients and programs. You work with deal teams and the sales teams to create the right solution for the clients and you ensure proper alignment of resources to deliver. You interface with our global customers, our sales and delivery teams to generate ideas and propose programs. You lead the charge to deliver solutions to these global customers. • You lead and grow our newly formed consulting practice in the CrossLab Enterprise space. This is a growing area for us and includes data analytics, Lean 6Sigma, Lab Ops Consulting; we see this growing into other areas. You will have the vision to create this space and implement business models to deliver high value to our enterprise customers. Specific responsibilities include, but are not limited to: • Manage a global team of consultants in the areas of data analytics, Lean 6Sigma and general laboratory operations. Work with our global sales and delivery teams to ensure that the team is integrated with them in the delivery of consulting services. • Manage accounts and programs in scope of responsibility • Develop trusted relationships with decision makers in each account, understand their strategic goals, and develop plans to partner on these goals. • Introduce new features, programs and best practices to customers. • Develop new materials - presentations, best practices, rollout plans, proposals, etc. - as needed. • Track and report on key metrics for customer success. • Ensures the program / account service business system is operating as expected, takes corrective action as appropriate and mitigates risks to Agilent’s performance (Customers, Shareholders and Employees). Proactively manages the resources to deliver upon the business needs. • Formally reviews business operations to ensure brand, culture and strategic objectives are achieved • Develops and implements organizational structure including the development of next generation of service/business leaders • Maintains strong alliances with key customers at account / program (Internal/External) in order to execute the business strategies • Actively fosters a quality and continuous improvement culture within the organization Qualifications • Bachelors or Masters degree plus demonstrated industry experience in large account and cross functional program management; integrating the resources of several complex departments, sites or functions. • Service business system understanding and expertise • Financial understanding of service operations • General understanding of Agilent products and markets • Customer Experience advocacy • Strong Communication skills • Results orientation / accountability • Demonstrated skill in teamwork within an organization and across functions and/or sites • Demonstrated skill in program management, strategic planning and tactical execution • Ability/experience to work across different countries and cultures • Highly developed interpersonal skills—someone who can be as effective through influence as through direct control. • Proven verbal and written communication skills • Experience with Analytical laboratory equipment, and Agilent products, is not required but highly desirable. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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4. Global Media Performance Manager – Englewood, CO
Req ID: 2066149 Locations: Englewood,Colorado,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Global Media Performance Manager Agilent is a leader in life sciences, diagnostics and applied chemical markets. The company provides laboratories worldwide with instruments, services, consumables, applications and expertise, enabling customers to gain the insights they seek. Agilent’s expertise and trusted collaboration give them the highest confidence in our solutions. Agilent’s culture is based on innovation; trust, respect and teamwork; and uncompromising integrity. Added to these are speed, focus and accountability to meet customer needs and create a culture of performance that draws on the full range of people's skills and aspirations. Agilent is regularly recognized by external organizations for its culture as well as its practices around processes and people. Agilent is seeking a Global Media Performance Manager to accelerate the advancement of its paid media strategy, planning and execution approaches across channels. This position sits within the newly formed Digital Marketing Center of Excellence, where the charter is to accelerate lead-to-revenue management and deliver positive ROMI for the company. The Global Media Performance Manager will play a pivotal role in enabling the company’s Digital Channel strategy and establishing a performance-driven culture across all marketing programs and campaigns. The ideal candidate will be well-versed in integrated marketing planning, advanced media strategies and tactics, as well as the technical platform capabilities needed to fully support a high-performing, data-driven media operation. Experience aligning internal stakeholders and managing external partners is essential. Key Responsibilities 1. Be an evangelist and champion of digital marketing performance. Help marketing teams fully utilize their budgets to develop the most exceptional plans and results-driven media campaigns possible. 2. Drive ROMI (return on marketing investment) globally for all of Agilent’s paid media channels (print, search, display, trade, social, etc.), while working in close partnership with external agency. Hold agency accountable for results. 3. Define ideal budget allocations across channels and the KPIs required to achieve individual program/campaign effectiveness and efficiency targets. Assist marketing teams in defining reach and sufficiency targets in order to accelerate conversion. Benchmark performance against competitors and industry best practices. 4. Drive adoption of marketing attribution, advanced segmentation and conceptual understanding of marketing mix modeling. 5. Leverage best in class Customer Experience and Digital Marketing practices (journey maps, buyer archetypes, personas, funnel stages, integrated marketing planning, rich media, dynamic ads, look-alike modeling/targeting, conversion optimization, programmatic buying, DMPs, 3rd party data, etc.) to deliver high-performing campaigns based on customer needs. 6. Discover audience insights that help identify common triggers and barriers to purchase, as well as points of receptivity, in order to build the most effective media strategies and segmentation models. 7. Develop playbooks, media kits, workflows and SLAs for stakeholder organizations. Provide governance over media operations. 8. Partner with Analytics COE, Marketing Technology and Product Managers with regard to end-to-end conversion tracking and digital platform requirements: AdWords, DoubleClick, Google Analytics, Call Tracking, Oracle Marketing Cloud, Dashboards, Reports, etc. Recommend additional technologies as needed. 9. Showcase best in class campaign results to the broader organization in order to elevate Agilent’s performance across all paid media channels. Geographical Location: Preferred location is Englewood, CO. Qualifications • 8+ years’ experience in media strategy, operations and innovation • Demonstrated success in establishing a data-driven, high-performing digital culture • Creative problem solver with ability to gain cross-functional alignment • Highly developed interpersonal skills and succinct communications; ability to translate hard data into an engaging narrative. • Deep understanding of creative best practices, A/B & MVAR testing, data analysis and digital marketing tools and platforms • Bachelor’s Degree or equivalent, MBA preferred Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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5. Life Science/ Chemical Analysis – Melville, New York
Req ID: 2063433 Locations: Melville,New York,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Intern Agilent's Life Science/ Chemical Analysis Group (LSCA) is a leading provider of analytical instrument systems that enable customers to identify, quantify, analyze and test the molecular, physical and biological properties of thousands of substances and products. LSCA has five sites worldwide: Waldbronn in Germany, Little Falls and Palo Alto in the USA, Tokyo in Japan, and Shanghai in China. As part of a highly qualified team of hard working and fun loving engineers you are the backbone of our great company by making sure that we stay ahead of the competition and keep on reaffirming our name as a global leader in test & measurement equipment. Part of that position we thank to our ability to provide customers with a superb support team that quickly responds to any issues they may have. Our customer satisfaction rates set us apart from the competition. As a recent graduated in Chemistry, Biochemistry or Biology you have the responsibility of supporting our clients for on-site installation, implementation, maintenance and repair of many of the quality products that we manufacture and sell. This can be very complex multimillion dollar projects around LC, LC/MS, GC, GC/MS instruments etc. complete with the appropriate software solutions. Additionally you can tweak your consulting skills and improve customer satisfaction by proactively advising customers on preventive maintenance and configurations, which may impact product performance. We will make sure you get all the training and development opportunities you need to become the best in your field. Qualifications To be really successful in the internship, you need to be enrolled in a University Degree program in Chemistry, Biochemistry or Biology although your proactive approach, team spirit and eagerness to build your sales knowledge are what will ultimately drive your success. You enjoy being in front of customers and supporting them while demonstrating your technical expertise. Interested in joining the world’s leading test & measurement company and you have what it takes for such an exciting internship, than don’t hesitate to apply! Agilent is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to disability, protected veteran status or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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6. Life Science/ Chemical Analysis – Cambridge, MA
Req ID: 2063434 Locations: Cambridge,Massachusetts,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Intern Agilent's Life Science/ Chemical Analysis Group (LSCA) is a leading provider of analytical instrument systems that enable customers to identify, quantify, analyze and test the molecular, physical and biological properties of thousands of substances and products. LSCA has five sites worldwide: Waldbronn in Germany, Little Falls and Palo Alto in the USA, Tokyo in Japan, and Shanghai in China. As part of a highly qualified team of hard working and fun loving engineers you are the backbone of our great company by making sure that we stay ahead of the competition and keep on reaffirming our name as a global leader in test & measurement equipment. Part of that position we thank to our ability to provide customers with a superb support team that quickly responds to any issues they may have. Our customer satisfaction rates set us apart from the competition. As a recent graduated in Chemistry, Biochemistry or Biology you have the responsibility of supporting our clients for on-site installation, implementation, maintenance and repair of many of the quality products that we manufacture and sell. This can be very complex multimillion dollar projects around LC, LC/MS, GC, GC/MS instruments etc. complete with the appropriate software solutions. Additionally you can tweak your consulting skills and improve customer satisfaction by proactively advising customers on preventive maintenance and configurations, which may impact product performance. We will make sure you get all the training and development opportunities you need to become the best in your field. Qualifications To be really successful in the internship, you need to be enrolled in a University Degree program in Chemistry, Biochemistry or Biology although your proactive approach, team spirit and eagerness to build your sales knowledge are what will ultimately drive your success. You enjoy being in front of customers and supporting them while demonstrating your technical expertise. Interested in joining the world’s leading test & measurement company and you have what it takes for such an exciting internship, than don’t hesitate to apply! Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws
Please have all applicants apply at www.jobs.agilent.com
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7. Multivendor Services Program Manager – Santa Clara, CA
Req ID: 2065292 Locations: Santa Clara,California,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Multivendor Services Program Manager Multivendor Services Program Manager, Laboratory Enterprise Division Multivendor Instrument Services is a foundational element of the LED service portfolio, providing comprehensive coverage of lab equipment across the customer's enterprise. The successful candidate will design strategies to manage complex lab instrumentation, commercialize product offerings using a rigorous product life cycle process, and oversee the launch and ramp to volume of those products. All this will be accomplished working in a dynamic, cross-functional team environment. Qualifications Qualifications: Bachelor's degree in Business, Marketing, or applicable Science discipline; MBA preferred 7+ years’ experience in technical product marketing position within a laboratory-related business; laboratory instrumentation and Service experience a plus Experience with both inbound and outbound marketing processes Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
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8. Global Compliance Services Program Manager – Santa Clara, CA
Req ID: 2065832 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Product Manager- Global Compliance Services Global Compliance Services Program Manager The Agilent CrossLab Group is looking for a Global Compliance Services Program Manager to lead the regulatory compliance services program. We are looking for an innovative leader to set a vision, collaborate with management and drive worldwide results for the program. Success in this role is ultimately measured by meeting the growth and profitability targets of the entire compliance portfolio. The Global Compliance Services Program Manager is a key member of the ACG Marketing Organization, the strategic leader of the portfolio. You will set direction for both the enterprise level and transactional aspects of the business. You will be responsible for the future vision of the compliance portfolio, leading the team on a multi-year journey into new markets. You will use customer research and market studies to help uncover new product needs, develop the business cases for new products, and work with the compliance product manager and outbound team on strategy for new product launches. Working with the compliance thought leaders, instrument product lines, software teams, field sales, and service deliver teams; you will be responsible to help compliance products achieve their targets. The ideal candidate will require excellent leadership and communication skills. You must demonstrate the ability to influence all levels of an organization, across regional/cultural boundaries and across multiple disciplines. You should have a strong background in product marketing, experience in the life science and analytical industry, and good knowledge of the regulatory compliance market. You will be dealing with a global organization requiring flexibility in work hours and the ability to travel. Major Responsibilities: • Achieve deep insights of customers and the competitors in regulated industries • Manages the customer and market research in support of the program • Sets the vision and 3-year strategy for Agilent CrossLab's compliance program • Collaborates with Agilent product line managers to develop a roadmap of compliance services • Develops the business case and drives development of new compliance services • Works with Global Marketing and Worldwide Field Sales to introduce new compliance services • Collaborates with R&D and the compliance product manager to set requirements for Agilent's Automated Compliance Engine (service delivery tool) • Coordinates the development of new processes for the sales and delivery of compliance services Qualifications Key Qualifications: Bachelor’s degree in life science, biology, chemistry, or related scientific field, MBA preferred 5+ year of product management experience Experience in the life science, diagnostics, and/or analytical chemistry markets • Track record of proven results to lead cross-functional marketing programs • Excellent verbal and written communications skills • Ability to travel (domestic and international) up to 20% of time Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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9. Project Manager/Data Analyst – Business Analytics – Wilmington, DE
Req ID: 2065500 Locations: Wilmington, Delaware,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Project Manager/Data Analyst – Business Analytics Agilent Technologies has long been a market leader in laboratory hardware in the life science and chemical analysis space. This is an opportunity to join our rapidly growing CrossLab services group and work on the next generation of data based laboratory management services. Deliver the promise of Big Data! Deliver services to our customers that manipulate, merge, and mine large and complex data sets (structured and unstructured) from diverse sources, to help those customers drive appropriate business actions based upon solid evidence. The project manager/data analyst for business intelligence will play the following roles – • Become an expert and train and support internal customers and engineers in our service delivery organization in the suite of data based business intelligence products we are developing. • Lead and participate in beta tests and pilots of new business intelligence services. • Manage escalations with these services and drive requirements and issues back into the IT organization responsible for the underlying data framework and toolset. • Lead cross functional teams to define and execute the business processes required to deliver these services and scrub and refine our databases. Qualifications - Bachelors or equivalent in Math, Computer Science, or Other technical degree. - Experience working on business analytics/intelligence preferably in a large organization, in a role between software engineering and the end consumer of business data. - Skill in the manipulation of large complex data sets, knowledge of one or more database query tools e.g. SQL, Brio, familiarity with statistical analysis e.g. hypothesis testing, regression, cluster analysis etc - Demonstrated experience and ability to lead cross-functional projects and develop organizational metrics. - Proven ability to work successfully in a team and take leadership in solving difficult situations. - Networking capabilities within multi-national, cross-organizational and geographically distributed teams. - Excellent oral and written communication skills. - Strong customer focus and/or experience in a customer facing role. - Ability to explain complex technical matters to a non-expert audience. -Knowledge of laboratory analytical equipment and Agilent’s pharmaceutical and chemical markets would be an advantage but is not a requirement for this position as well as experience in a service delivery organization. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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10. Service Business Manager - Puerto Rico
Req ID: 2065247 Locations: San Juan,Puerto Rico,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Puerto Rico is the fastest growing territory on AFO and requires an active, skilled and proactive collaborator that can continue the excellent work done so far. Puerto Rico is a district that has primarily pharmaceutical accounts that are demanding with quality of services and high level of partnership. In addition, this territory is an excellent arena for CrossLab initiatives for becoming the true business partner of our customers. Do you like this challenge? •Service Business Manager is responsible for leading the team responsible for implementation of support delivery programs/ processes (installations, repairs, maintenance, hardware and software, applications and customer training), coordinate their technical development and any other skills that helps them to deliver the best interaction. •Manages the Service Business using financial and operational metrics (including customer satisfaction) as the compass on the journey. •Service Business Manager administer resources to implement tactical business plans and programs/ projects for improving quality of services, special programs at key accounts, market strategies for growing and winning in the service market. •Is also the leader for the Authorized Service Partner program on Puerto Rico as part of the tactical plan to deliver above both customer expectations and market average •Should be a strong collaborator with CCCC and team work on designing the best strategy for receiving customer request and transform it on the best experience possible. •Develops, implements solutions to department issues, team works with Instrument Sales and Consumable sales for a unified strategy on Puerto Rico Service Manager responsible for this district should have the following skills: • Negotiation • Clear and effective communication • Customer Orientation • Analytical mind set • Planning and executing, results oriented Geographical Location: Puerto Rico preferred. Limited relocation funding. Qualifications • Very desirable to live out or relocate to Puerto Rico. • Solid Bilingual skills both written and verbal. • Strong Communicator, able to create a compelling presentation to support business goals and get buy-in for ideas, inspire others to achieve better results. • Leadership skills, able to set priorities, delegate, motivate and develop others. • Collaboration skills, value and celebrate differences, build rapport, form alliances and negotiate effectively. • Able to understand financials and weight implication of decisions on this area • Desirable knowledge of Customer Service Organization processes • Master Degree or University Degree or equivalent • 3 years directly relevant experience as a manager, supervisor and/or individual contributor within analytical instrumentation industry. Experience in a Customer Service Organization either as individual contributor or supervisor/manager preferred. • Requires proven skills in leading/managing the execution of processes, projects and tactics. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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11. QQQ LC/MS Lead Instructor – Lexington, MA
Req ID: 2065494 Locations: Lexington,Massachusetts,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group QQQ LC/MS Lead Instructor Agilent is a leader in life sciences, diagnostics and applied chemical markets. The company provides laboratories worldwide with instruments, services, consumables, applications and expertise, enabling customers to gain the insights they seek. Agilent’s expertise and trusted collaboration give them the highest confidence in our solutions. Agilent’s culture is based on innovation; trust, respect and teamwork; and uncompromising integrity. Added to these are speed, focus and accountability to meet customer needs and create a culture of performance that draws on the full range of people's skills and aspirations. Agilent is regularly recognized by external organizations for its culture as well as its practices around processes and people Join the team that is leading the solutions revolution at Agilent. In this QQQ LC/MS lead instructor position for the AFO Education & Consulting Solutions team, you will be responsible for delivering training and consulting that help customers realize their business outcomes. You will set strategy for the delivery of training and consulting in your technique and mentor both internal & external QQQ LC/MS delivery resources to ensure they have the technical competency required to achieve a "best in class" customer experience. You will also participate in the design and management of the new LC/MS training center in Lexington, MA scheduled to open in June 2016. This fast paced and dynamic team is looking for like-minded technical professionals that are customer focused and have a passion for teaching. Key Responsibilities • Delivery of ECS sanctioned events including but not limited to: Standard training courses On-site custom training vILT sessions Consulting engagements per demand in area of expertise • Manage technical expertise for all contractors providing training/consulting in the technique Arrange update training/ NP training as needed for the business Review Customer Satisfaction metrics for each contractor - corrective action if required Perform yearly reviews • Identify and On-board delivery resources as needed to support the business Contractors FTE • Schedule yearly calendar and teaching assignments for each planning cycle Partner with other Leads and logistics staff to ensure calendars are aligned and supportable with current assets and training space Plan resource utilization to maximize customer satisfaction and program profitability • Assist in development and testing of new course material • Participate in Agilent University (AU) technical communities as moderator • Mentor delivery resources on best practices of AU for a consistent and excellent customer experience including: Training resources on new delivery modalities Auditing courses to ensure compliance with best practices • Manage the new LC/MS training facility in Lexington, MA ( June 2016) Oversee equipment performance and Pm schedules Order consumables, chemicals and supplies required to conduct customer training classes Ensure AU best practices are followed by all instructors performing training at the site. Work with the North America lab manager for capital asset purchases and technology refresh. Qualifications • Bachelors or Master Degree or University Degree or equivalent plus a minimum of 8 years relevant experience. • Post-graduate and/or certification / license may be required. • Proven proficiency in the operation of Agilent QQQ LCMS platforms. • Demonstration of excellent communication and teamwork skills • Proven lecture & presentations skills both in a classroom environment and virtually are required. • Previous supervisory experience such as team lead or project lead is desired. • Video submission of instructing style may be required, if selected for final interview. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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12. R&D Materials Scientist – Santa Clara, CA
Req ID: 2065843 Locations: Santa Clara,California,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Researcher - R&D Materials Scientist Agilent is the premier laboratory partner for a better world. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the insights they seek – so they can do what they do best: improve the world around us. Information about Agilent is available at Agilent.com. This position is part of a dynamic multidisciplinary R&D team that develops state‐of‐the‐art technologies to advance the capabilities of life science and chemical analysis instrumentation through use of novel materials, coatings and microfabrication. The successful candidate will be a scientist with proven leadership capability who performs research and development to create novel functional coatings and surface modifications. The role requires someone with strong technical skills in a range of surface analytical techniques, such as XPS, AES and FTIR, as well as extensive practical knowledge of the physical, chemical and mechanical behavior of materials and thin films. The candidate must have exceptional problem solving skills, be able to quickly adapt to the demands of rapidly changing multifaceted projects, and have the technical and leadership skills to initiate collaborations with world-class colleagues, both internal and external. Qualifications Qualifications: - Ph.D. in Materials Sciences, Engineering, Physics, Chemistry, or related discipline - Strong technical skills in multiple surface characterization techniques such as XPS, Auger, AFM, FTIR, ellipsometry, etc. - Strong theoretical and practical knowledge of thin films and materials, including biomaterials - Demonstrated capability in solving complex materials problems through targeted use of characterization techniques - Excellent oral and written communication skills; demonstrated leadership success in a collaborative multidisciplinary environment The following additional skills/experiences are highly desired: - Experience with surface modification for biocompatibility Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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13. Researcher - R&D Thin Films – Santa Clara, CA
Req ID: 2065011 Locations: Santa Clara,California,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Researcher - R&D Thin Films Agilent is the premier laboratory partner for a better world. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the insights they seek – so they can do what they do best: improve the world around us. Information about Agilent is available at Agilent.com. As a successful candidate you will join a dynamic multidisciplinary R&D team developing state‐of‐the‐art technologies that advance the capabilities of life science and chemical analysis instrumentation through innovative use of novel materials, coatings and microfabrication. We are seeking expertise in coatings and thin film deposition to create advantageous surface properties of key components to impact the performance, efficiency, and lifetime of these tools. Successful integration of surface analysis and other characterization will be essential for this role. This position requires a candidate with exceptional agility and problem solving skills, someone who can quickly adapt to the demands of rapidly developing, multifaceted projects and work in collaboration with world-class colleagues, both internally and externally, through partnerships and collaborations. The ideal person will combine initiative, collaboration and creativity to transform analytical capabilities that enable our customers to achieve discoveries that improve the quality of life. Qualifications - - Ph.D. in Materials Sciences, Engineering, Physics, Chemistry, or related discipline - Hands-on experience with vapor phase coating techniques such as CVD, ALD, MOCVD, etc. - Demonstrated proficiency with surface analysis techniques such as XPS, Auger, EDS, AFM, FTIR, etc - Strong analytical skills and decision making ability - Excellent communication and teamwork skills; demonstrated success in a multidisciplinary environment - Record of impactful publication and innovation using surface coating or modification for novel applications The following additional skills/experiences are highly desired: - Experience with microfabrication techniques such as lithography, wet chemical etching, plasma etching, plasma deposition and sputter deposition. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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14. Senior Level Quality Assurance Engineer - Chemistries and Supplies – Folsom, CA
Req ID: 2066070 Locations: Folsom,California,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Senior Level Quality Assurance Engineer - Chemistries and Supplies We are seeking an enthusiastic, people-oriented, Quality Assurance Engineer for our Consumables and Supplies business at our Folsom, California site. Folsom is a growing state-of-the-art production and manufacturing facility focusing on market-leading gas chromatography and sample preparation consumables products. These are high-visibility product lines where you will have the opportunity to make a real difference in one of Agilent's key businesses. Key Responsibilities: -Consult with engineers in R&D and Manufacturing on the design of new products to meet compliance and quality objectives of performance, reliability, manufacturability, usability, supportability and annual failure rate. -Work and communicate in a worldwide, cross-functional team environment that includes R&D, marketing, manufacturing, procurement, and supply chain. -Provide Quality function support, such as writing quality plans, providing quality testing and representing Quality on new product introductions and engineering changes. -Lead quality plans and requirements and foster an environment of continuous improvement. -Identify and lead resolution of quality and customer satisfaction issues. -Ensure ISO 9001 compliance through internal and external audits. -Record, analyze and distribute statistical information. -Available for approximately 10% business travel. Qualifications Required Skills: - 8+ years of experience in Quality Assurance - Bachelors or Master Degree or University Degree or equivalent in Chemistry, Materials Science, or Engineering -Experience with ISO 9001 highly desired. ISO 13485 preferred but not required -Must have a desire for achieving excellence in customer satisfaction, process, and product quality and reliability -Strong analytical skills and excellent problem solving abilities -Ability to multi-task several assignments at a time, prioritize key issues, and deliver on commitments. -Excellent verbal and written communication skills. Must be extremely detail-oriented with respect to documentation and communication -Self-starter, able to take initiative -Knowledge of chemical, safety, environmental and regulatory guidelines -Experience with Six Sigma and/or Lean methodologies -Knowledge of product regulations including chemical, safety, EMC, and environmental standards -Quality Engineering experience as needed for new product introductions, such as writing quality plans, quality testing and representing QA on new product introductions project management -Familiarity with Product Lifecycle Process, Corrective and Preventative Action Process (CAPA), Customer issue resolution processes Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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15. Senior Service Engineer- LCMS – Boston, MA
Req ID: 2064986 Locations: Boston,Massachusetts,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Senior Service Engineer- LCMS In the role of an Agilent Field Service Engineer (FSE) your primary responsibility will be providing on-site installations, maintenance, qualifications and repairs of Agilent and multi-vendor system solutions. Typical analytical products supported include LC, GC, MS, ICPMS, UV/VIS and Data Systems. The primary area of product focus in this role will be on high-end LCMS (TOF, QTOF and QQQ). This position is primarily responsible for supporting a customer install base extending throughout New England. However, it is not uncommon to routinely perform service activities in neighboring districts or occasionally throughout the U.S. as needed. In addition to those activities defined above, the successful candidate will be responsible for the following: - Establishing and maintaining a highly responsive relationship and effective communication with customers, sales reps, peers and other departments within Agilent to ensure customer satisfaction. - Setting clear customer expectations and following through on commitments associated with all service activities. - Ensuring customer satisfaction by advising customers on preventive maintenance and configurations, which may impact product performance. This could include providing customer training as required. - Providing service in accordance to customer's entitlement (contract, warranty or trade). - Drive business results by actively participating in FSE Lead Programs with the intent of driving potential sales opportunities and increasing revenue. - Adhering to Agilent's business priorities associated with FSE utilization, call closure and parts inventory management. - Maintaining up to date technical knowledge for assigned products. - Partnering with colleagues and Agilent's Solution Unit acting as an internal resource on technical issues. - Adhering to environmental health and safety guidelines. - Diligent and accurate paperwork submissions, including Field Service Reports, Qualification protocols, PM checklists and internal documentation requirements. The above responsibilities are intended to describe the general nature and level of work performed by the successful candidate. They are not intended to be an exhaustive list of all duties and responsibilities. Qualifications BS Degree in Sciences (Chemistry, Biology, etc.) or equivalent work experience and a minimum of 8 years related hands-on experience with analytical instrumentation. - High-end LCMS (TOF, QTOF and QQQ) experience a must. Can be with Agilent or other OEM instrumentation. - Proven track record of successful field customer management. - Strong organizational and leadership capabilities. - Excellent verbal and written communication skills are a must. - Demonstrated ability to perform hands on maintenance, installations and selected repairs on analytical instruments. - Ability to solve, high impact problems related to product availability; typically system/solution focused. - Must be available for up to 25% travel that may include over-night stays. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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16. Senior Service Engineer- LCMS – Boston, MA
Req ID: 2064987 Locations: Boston,Massachusetts,United States,Americas Relocation Benefits: YES Business: Agilent CrossLab Group Senior Service Engineer- LCMS In the role of an Agilent Field Service Engineer (FSE) your primary responsibility will be providing on-site installations, maintenance, qualifications and repairs of Agilent and multi-vendor system solutions. Typical analytical products supported include LC, GC, MS, ICPMS, UV/VIS and Data Systems. The primary area of product focus in this role will be on high-end LCMS (TOF, QTOF and QQQ). This position is primarily responsible for supporting a customer install base extending throughout New England. However, it is not uncommon to routinely perform service activities in neighboring districts or occasionally throughout the U.S. as needed. In addition to those activities defined above, the successful candidate will be responsible for the following: - Establishing and maintaining a highly responsive relationship and effective communication with customers, sales reps, peers and other departments within Agilent to ensure customer satisfaction. - Setting clear customer expectations and following through on commitments associated with all service activities. - Ensuring customer satisfaction by advising customers on preventive maintenance and configurations, which may impact product performance. This could include providing customer training as required. - Providing service in accordance to customer's entitlement (contract, warranty or trade). - Drive business results by actively participating in FSE Lead Programs with the intent of driving potential sales opportunities and increasing revenue. - Adhering to Agilent's business priorities associated with FSE utilization, call closure and parts inventory management. - Maintaining up to date technical knowledge for assigned products. - Partnering with colleagues and Agilent's Solution Unit acting as an internal resource on technical issues. - Adhering to environmental health and safety guidelines. - Diligent and accurate paperwork submissions, including Field Service Reports, Qualification protocols, PM checklists and internal documentation requirements. The above responsibilities are intended to describe the general nature and level of work performed by the successful candidate. They are not intended to be an exhaustive list of all duties and responsibilities. Qualifications BS Degree in Sciences (Chemistry, Biology, etc.) or equivalent work experience and a minimum of 4 years related hands-on experience with analytical instrumentation. - High-end LCMS (TOF, QTOF and QQQ) experience a must. Can be with Agilent or other OEM instrumentation. - Proven track record of successful field customer management. - Strong organizational and leadership capabilities. - Excellent verbal and written communication skills are a must. - Demonstrated ability to perform hands on maintenance, installations and selected repairs on analytical instruments. - Ability to solve, high impact problems related to product availability; typically system/solution focused. - Must be available for up to 25% travel that may include over-night stays. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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17. Services Product Manager – Santa Clara, CA
Req ID: 2065456 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Services Product Manager As the Services Product Manager you will be working with a team of product managers responsible for a portfolio of service products. You will be involved in the market research of new ideas, design and development of new offerings, projects to optimize of the business model, pricing of services, and the development of marketing programs to insure a profitable revenue stream for the product line. The role also includes leading marketing projects, working on cross-functional project teams, and working with instrument product managers across the company to attach relevant services to their products. We are looking those who are innovative, flexible, and exhibit a high degree of collaboration. We are looking for graduates located in San Jose, California or Wilmington, Delaware areas. Qualifications • Strong evidence of skills in business and product marketing • Highly desired – MBA or marketing experience • Preference for bachelor’s degree in chemistry, life science or related engineering • Familiar with life science and analytical chemistry instrumentation • Excellent skills in Excel spreadsheets and financial analysis tools • Strong evidence of customer focus and teamwork • Excellent verbal & written communication skills • Ability to travel up to 10% Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws
Please have all applicants apply at www.jobs.agilent.com
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18. Software Application Specialist – Carpinteria, CA
Req ID: 2065068 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Software Application Specialist Diagnostic Services is looking for an experienced technology leader with a strong medical device hardware and software background to deliver technical support activities for our pathology/histology instrumentation solutions. We develop pathology solutions for tissue-based cancer diagnostics. Our portfolio of solutions include fully automated systems, all operating in a highly-regulated market environment. We are using lean lab approaches to increase our customer's productivity and efficiency while simultaneously eliminating the chances of operational errors in their workflows. This is an opportunity to join an enthusiastic and dynamic team and work closely with application experts, hardware experts, marketing, QA/RA and directly with customers. Responsibilities include: - Provides through telephone or other communication tools general information of a technical and occasionally non-technical nature, to Agilent existing and potential customers. - Monitor Service help desk and phone queue to respond to inquiries and requests for support. - Document all complaints or reportable events per QMS procedures. - Provides escalation support to internal resources including Technical Support, Field Service and Application Specialists. - Troubleshoot IT and instrument issues using various methods including remote access and reviewing the instrument's diagnostic files. - Serve as a primary conduit of information back to global IT team for troubleshooting, problem investigation and resolution of instrument hardware and software issues. - Evaluates assignments and determines actions required to provide technical support service. - Duties involve analysis and new/ customized approaches. - Solves complex problems requiring technical and business admin breadth/ depth of knowledge. Qualifications Qualifications: - Bachelor’s degree, specialized training/certification, or equivalent combination of education and experience. - 5+ year’s relevant experience in similar position. - Extensive troubleshooting knowledge and skills to complete specialized tasks. - Experience with Laboratory Information Systems, Laboratory Equipment, Laboratory Workflow, Networks and Server Administration is a plus GEO Location: Carpinteria, California Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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19. Technical Support Specialist – Carpinteria, CA
Req ID: 2065613 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Agilent CrossLab Group Technical Support Specialist About Dako, an Agilent Technologies Company: Dako, based in Denmark, is a global leader in tissue-based cancer diagnostics. Hospital and research laboratories worldwide use Dako’s reagents, instruments, software and expertise to make precise diagnoses and determine the most effective treatment for cancer patients. Dako, with 1,100 employees, operates in more than 100 countries. Dako became part of Agilent Technologies on June 21, 2012. www.dako.com About Agilent Technologies: Agilent Technologies Inc. (NYSE: A) is the world’s premier measurement company and a technology leader in chemical analysis, life sciences, diagnostics, electronics and communications. The company’s 20,000 employees serve customers in more than 100 countries. Agilent had net revenues of $6.6 billion in fiscal 2011. www.agilent.com Position Summary In this position you will provide technical support for our customers (internal and external). Insure that all regulatory, policies, and goals are met. Maintain customer relations and insure customer satisfaction with service. Complete all administrative duties as required. This position works directly with tissue diagnostic IVD medical devices in hospitals and laboratories. Responsibilities • Monitor Service Help Desk and Phone Queue to respond to inquiries and requests for technical support to Agilent existing and potential customers. • Troubleshoot Dako’s line of products and systems • Research required information using available resources • Document all complaints or reportable events per QMS procedures. • Follow standard processes and procedures • Provide escalation support to internal resources including Technical Support, Field Service and Application Specialists. Qualifications Qualifications: • Bachelor’s degree, specialized training/certification, or equivalent combination of education and experience. • 5+ year’s relevant experience in similar position. • Extensive troubleshooting knowledge and skills to complete specialized tasks. • Experience with Laboratory Information Systems, Laboratory Equipment, Laboratory Workflow, Networks and Server Administration is a plus • Ability to work with minimal supervision and show sound business judgment with regard to escalating issues when the managers help is needed to make a decision. Other Qualifications: • Proficient in Windows OS, and Microsoft Office • Proper phone etiquette • Flexible and open to change; detail oriented • Ability to multi-task in a fast paced environment
• Ability to solve complex problems dealing with a variety of variables • Ability to write reports, technical correspondence and procedures • Ability to effectively present information and respond to questions from internal and external customers as well as management • Computer hardware and network experience a plus • Ability to function in a responsible, professional manner using good judgment in decision making. Requires the ability to remain positive, rational, calm and professional under stressful conditions (I.e. dealing with irate people, handling complaints, etc.) GEO Location: Carpinteria, California Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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20. OF & Supply Chain Associate Scientist- Cedar Creek, TX
Req ID: 2064804 Locations: Cedar Creek,Texas,United States,Americas Relocation Benefits: NO Business: Agilent OF & Supply Chain Associate Scientist- Reagent Manufacturing As a Manufacturing Associate you will be a member of the Reagents manufacturing team. In this role, you will join a dynamic biological manufacturing team (Reagents) within Agilent Technologies. You will have the opportunity to work independently as well as part of a team to ensure the efficient production and quality control of life science products. The ideal candidate will also have proven proficiency in molecular biology techniques including but not limited to: end-point and real-time PCR, DNA/RNA extraction and purification, gel electrophoresis and other nucleic acid-based technologies. You will have the keen ability to perform these tasks while adhering to industry and government standards regarding proper laboratory techniques and safe handling of biohazardous and radioactive materials. You will be measured on your ability to conduct the manufacturing and analysis of materials for the qualification of PCR related kits, with limited supervision. Manage laboratory supplies and inventoried materials and maintain diligent records of data and processes. Other duties may include the writing, maintenance and reviewing of ISO compliant work instructions (WI) and standard operating procedures (SOP). Expect to assist in the trouble shooting of technical problems that may arise. Qualifications This position requires a BS/BA degree in biological science and/or equivalent education and related field and two (2) to four (4) years of previous experience in chemistry, molecular biology, and/or biochemistry OR a Masters in biological science or related field and one (1) to two (2) years of previous experience in chemistry, molecular biology, and/or biochemistry. Must have hands on working knowledge of standard laboratory techniques of molecular biology (PCR, QPCR, cloning, enzymatic assays, DNA/RNA purification, and array technology). Strong oral and written communication, organization, team building and computer skills essential to the role. Geo Location:Cedar Creek, TX Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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21. OF & Supply Chain Commodity Manager – Wilmington, DE
Req ID: 2065302 Locations: Wilmington,Delaware,United States,Americas Relocation Benefits: YES Business: Agilent OF & Supply Chain Commodity Manager As a member of Agilent CrossLab Group Procurement team, the Commodity Manager proactively manages the relationships with suppliers to ensure product availability, quality and profitability meet the business' goals. In addition, the successful candidate will define and drive the commodity strategy to meet current and future business needs. The successful candidate will manage business aspects of his/her assigned commodity and act as the team lead working with the various partners to achieve the expected business results. Position Responsibilities/Duties: • Supply Market Analysis - Develop a strong understanding of the supply market, its capability, direction, trends, etc. - Understand who the best suppliers are; the niches they serve, their capability, etc. • Partner & BU Alignment - Develop strong understanding of business requirements. Work with partners to clearly understand their direction and needs. - Internalize the requirements and define what needs to be delivered to meet their needs, also identify additional opportunities to deliver new value-add. • Strategy Development - Work with management to translate the business requirements into objectives and goals for the commodity. - Lead the development of the commodity strategy. Develop the appropriate initiatives to achieve the strategy and meet business requirements. - Establish sourcing targets based on the business needs and requirements. Develop the appropriate sourcing strategy and initiatives and plans to meet and / or exceed the targets. • Supplier Evaluation & Selection - Evaluate production and R&D requirements. Determine if a current supplier can meet the needs. - Identify, evaluate and select new suppliers that meet Agilent's business requirements. - Conduct supplier audits to properly evaluate potential suppliers. - Ensure the right set of suppliers available when needed. - Prior to selecting a new supplier, assess the need for a contract, establish performance expectations, and review financial stability • Category Leadership, Analysis and Execution - Stay current with industry developments for the commodity. Conduct research using various sources such as trade journals, internet, ISM, business news and internal and external networking. Maintain a basic technical knowledge. - Maintain continuous assurance of supply (AOS) - serve as an escalation point for AOS issues. - As the commodity team leader, work with management to establish goals and objectives and drive to meet the goals as set at the Procurement (Business Fundamental Table) BFT level. - Help coach and train team members, build teamwork, lead team meetings and communicate important commodity related information, set priorities, track and report commodity team performance and business fundamentals, and drive for continuous process improvement. Help the management hold the team accountable for meeting commitments. • Contract Management - Identify critical parts and suppliers requiring contracts. - Review and discuss suppliers business recovery plans and succession plans to identify risk to Agilent. - Develop and negotiate the appropriate contracts to protect Agilent's interests; get the best total cost, and minimize business risk.
•Cost Management - Establish total cost of ownership targets based on business needs. Implements the appropriate initiatives to meet and/or exceed targets. - Conduct the appropriate analysis ('should cost models' or other forms of analysis) to ensure that the cost being paid has been analyzed and an external comparison of the product or some of the raw material or fabrication has been completed and what we are paying is inline or below the market. - Prepare and evaluate quotation packages. - Analyze variances for new parts/products. - Drive cost optimization throughout supply chain and provide reporting. •Supplier Performance Management - Execute supplier performance surveys, analyze data, and prepare supplier feedback. - Meet with management to share supplier results, plans and gain their support. - Meet with top suppliers at least annually to review direction, assure alignment, and review performance results. - Hold suppliers accountable for meeting commitments and performance expectations. - Work with suppliers to develop performance improvement plans (as needed) and monitor progress. Qualifications • Bachelors or Masters Degree or equivalent plus a minimum of 8 years relevant experience, with typically 10-14 years practical experience. • Effective communication skills and project management experience to lead cross-functional initiatives across various groups, sites and organizations. •Good Business Acumen with positive solutions-oriented approach and ability to build productive relationships. •Experience with employing various financial and analytical tools and processes to make appropriate business decisions, such as risk analysis, total cost analysis/cost models, Should Cost Models, competitor analysis, break-even analysis, Make vs. Buy analysis, and benchmarking. •Willingness and ability to travel internationally required. •Working knowledge of SAP or similar ERP system desirable. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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22. OF & Supply Chain Commodity Manager – Wilmington, DE
Req ID: 2066020 Locations: Wilmington,Delaware,United States,Americas Relocation Benefits: YES Business: Agilent OF & Supply Chain Commodity Manager As a member of Agilent CrossLab Group Procurement team, the Commodity Manager proactively manages the relationships with suppliers to ensure product availability, quality and profitability meet the business' goals. In addition, the successful candidate will define and drive the commodity strategy to meet current and future business needs. The successful candidate will manage business aspects of his/her assigned commodity and act as the team lead working with the various partners to achieve the expected business results. Position Responsibilities/Duties: • Supply Market Analysis - Develop a strong understanding of the supply market, its capability, direction, trends, etc. - Understand who the best suppliers are; the niches they serve, their capability, etc. • Partner & BU Alignment - Develop strong understanding of business requirements. Work with partners to clearly understand their direction and needs. - Internalize the requirements and define what needs to be delivered to meet their needs, also identify additional opportunities to deliver new value-add. • Strategy Development - Work with management to translate the business requirements into objectives and goals for the commodity. - Lead the development of the commodity strategy. Develop the appropriate initiatives to achieve the strategy and meet business requirements. - Establish sourcing targets based on the business needs and requirements. Develop the appropriate sourcing strategy and initiatives and plans to meet and / or exceed the targets. • Supplier Evaluation & Selection - Evaluate production and R&D requirements. Determine if a current supplier can meet the needs. - Identify, evaluate and select new suppliers that meet Agilent's business requirements. - Conduct supplier audits to properly evaluate potential suppliers. - Ensure the right set of suppliers available when needed. - Prior to selecting a new supplier, assess the need for a contract, establish performance expectations, and review financial stability • Category Leadership, Analysis and Execution - Stay current with industry developments for the commodity. Conduct research using various sources such as trade journals, internet, ISM, business news and internal and external networking. Maintain a basic technical knowledge. - Maintain continuous assurance of supply (AOS) - serve as an escalation point for AOS issues. - As the commodity team leader, work with management to establish goals and objectives and drive to meet the goals as set at the Procurement (Business Fundamental Table) BFT level. - Help coach and train team members, build teamwork, lead team meetings and communicate important commodity related information, set priorities, track and report commodity team performance and business fundamentals, and drive for continuous process improvement. Help the management hold the team accountable for meeting commitments. • Contract Management - Identify critical parts and suppliers requiring contracts. - Review and discuss suppliers business recovery plans and succession plans to identify risk to Agilent. - Develop and negotiate the appropriate contracts to protect Agilent's interests; get the best total cost, and minimize business risk.
•Cost Management - Establish total cost of ownership targets based on business needs. Implements the appropriate initiatives to meet and/or exceed targets. - Conduct the appropriate analysis ('should cost models' or other forms of analysis) to ensure that the cost being paid has been analyzed and an external comparison of the product or some of the raw material or fabrication has been completed and what we are paying is inline or below the market. - Prepare and evaluate quotation packages. - Analyze variances for new parts/products. - Drive cost optimization throughout supply chain and provide reporting. •Supplier Performance Management - Execute supplier performance surveys, analyze data, and prepare supplier feedback. - Meet with management to share supplier results, plans and gain their support. - Meet with top suppliers at least annually to review direction, assure alignment, and review performance results. - Hold suppliers accountable for meeting commitments and performance expectations. - Work with suppliers to develop performance improvement plans (as needed) and monitor progress. Qualifications • Bachelors or Masters Degree or equivalent plus a minimum of 4 years relevant experience. • Effective communication skills and project management experience to lead cross-functional initiatives across various groups, sites and organizations. •Good Business Acumen with positive solutions-oriented approach and ability to build productive relationships. •Experience with employing various financial and analytical tools and processes to make appropriate business decisions, such as risk analysis, total cost analysis/cost models, Should Cost Models, competitor analysis, break-even analysis, Make vs. Buy analysis, and benchmarking. •Willingness and ability to travel internationally required. •Working knowledge of SAP or similar ERP system desirable. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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23. OF & Supply Chain Engineering Intern – Wilmington, DE
Req ID: 2065530 Locations: Wilmington,Delaware,United States,Americas Relocation Benefits: NO Business: Agilent OF & Supply Chain Engineering Intern This position is at our Little Falls, (Wilmington), Delaware site, located midway between Baltimore and Philadelphia. There, we have 800 people inventing, designing, building and marketing products that dominate the market for chemical analysis. Our products are frequently behind the headlines in the news, from environmental regulations to new drug discoveries to Homeland Security. You'll even see our instruments on television shows like "CSI". The Gas Chromatograph (GC) manufacturing engineering team is looking to hire Software/Computer/Electrical Engineering Intern to help with a number of S/W projects. Programming skills required in some of the following languages: C-Family (C, C++, Java, C#), Python, HTML, Visual Basic. • Production Test Assistance: Assist manufacturing and test engineer with development of GC Test software/software focusing on reduction of cycle times and yield improvement and help alleviate some of the daily production requests for test efficiency, low yield, and bug fixes. • NPI test development and validation: Work with a international team of NPI engineers to develop, setup, validate and qualify the testers for new product in NPI phase. • Automation support for engineering projects: Support the manufacturing engineer to design and setup automated tooling, measurement devices for engineering investigation and experimentation purposes. Qualifications As this is an Intern position, the job candidate must be pursuing a Bachelors or Master's Degree in Software Engineering, Computer Engineering, Computer Science, or Electrical Engineering and have experience in the following areas: •GPA requirements should be 3.0 or higher. •Programming skills required in some of the following languages: C-Family (C#, C++, Java), HTML, Visual Basic, Python. •Ability to communicate needs, plans and achievements at all levels of a corporate organization. •Demonstrated ability to set priorities and meet commitments. •Ability to simultaneously participate in multiple issues as they arise in a manufacturing environment. •Ability to work in a hands-on environment. •Ability to take on new challenges and learn from the experience of coworkers. •Experience scheduling and completing tasks on schedule. •Project coordination and management skills. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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24. OF & Supply Chain Manufacturing Chemist – Newport, DE
Req ID: 2064948 Locations: Newport,Delaware,United States,Americas Relocation Benefits: YES Business: Agilent OF & Supply Chain Manufacturing Chemist Agilent Technologies is seeking a Manufacturing Chemist to join their high-performance Engineering team working at the liquid chromatography column manufacturing plant in Newport, Delaware. Key responsibilities include: - Designing, improving, and troubleshooting the chemical processes and chemical process equipment for the production of silica based packing for high performance liquid chromatography columns. The Manufacturing Chemist with work in a dynamic production environment in collaboration with Product Line Engineers, QA Chemists, Production Supervisors, Manufacturing Technicians, Production Operators, and Maintenance Staff. This is not a laboratory based position. - Participating and supporting aspects of technology transfer and scale-up of manufacturing processes delivered from R&D and New Product Introduction teams into Engineering and Manufacturing. -Collaborating with Product Line Engineers, Analytical Chemists, and Marketing / Customer Service staff to draft quality documentation and specifications for raw materials, in-process/intermediate products, and final products. - Participating and supporting the Management of Change control process, determining disposition of nonconforming product, and creating and executing corrective and preventive action plans. - Occasionally writing standard operating procedures and training plant staff. - Analyzing process and quality data using statistical analysis tools, and maintaining metrics for the production process. - Collaborating with Agilent Sales, Marketing and Field Staff, or Agilent customers, to resolve technical issues with HPLC columns at customer sites. - Work as a project team leader, or participate on project teams, to achieve product and process improvements. Qualifications Requires: • Doctorate or Master’s Degree in Chemistry, or equivalent, or a combination of education and or experience. • More than 10 years of related experience as an organic chemist in a chemical manufacturing environment preferred. Knowledge of silica based chemistry and High Performance Liquid Chromatography is highly desired. •Ability to work as a successful project manager or member of a project team to achieve strategic goals while meeting schedules, budgets, and technical objectives. • Excellent communication and presentation skills. • Excellent skills in statistical analysis, Six Sigma, Lean Manufacturing, and operational trouble shooting. • Mechanically inclined. • Previous experience in an ISO9000 registered or FDA regulated manufacturing environment highly desired. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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25. OF & Supply Chain Manufacturing Operator – Santa Clara, CA
Req ID: 2064936 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Agilent OF & Supply Chain Manufacturing Operator Machine operator position to work on the "B" shift which is a 12hr AWS shift from 5:00pm to 5:00am. Scheduled work days are every Sunday, Monday, Tuesday & alternating Wednesday. Performs routine Microarray production and Fabrication duties to quality standards as defined by the department. Performs troubleshooting and verifies that product conforms with customer specifications. Maintains accurate reports and provides necessary documentation. Communicates with engineers, supervisors, technicians, order processing and others within the department to clarify customers' orders, give feedback on defects and/or quality of the product. Helps implement process/product improvements, etc. The above statements are intended to describe the general nature and level of work being performed by incumbents. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required by all incumbents. Incumbents may perform other duties as assigned in addition to the above. All Agilent employees are expected to: Promote teamwork and cooperative effort. Help train and give guidance to other Agilent employees. Maintain a clean, safe, and unobstructed work area, practices good safety habits, and utilize appropriate safety equipment. Provide customers with the highest quality products and service. Understand and apply appropriate quality improvement and Processes. Qualifications • Requires higher education or specialized training/certification, or equivalent combination of education and experience. • Typically minimum of 5 years relevant experience for entry to this level. Requires extensive knowledge and skills to complete specialized tasks. • Experience working within an ISO13485 quality system desired. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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26. OF & Supply Chain Manufacturing Software Implementation Engineer – Wilmington, DE
Req ID: 2065434 Locations: Wilmington,Delaware,United States,Americas Relocation Benefits: YES Business: Agilent OF & Supply Chain Manufacturing Software Implementation Engineer This position is at our Little Falls, (Wilmington), Delaware site, located midway between Baltimore and Philadelphia. There we have 800 people inventing, designing, building and marketing products that dominate the market for chemical analysis. Our instruments are frequently behind the headlines in the news, from environmental regulations to new drug discoveries to Homeland Security. You'll even see our instruments on television shows like "CSI". Principal Duties and Responsibilities: - Analyze, solution design and execute design, development and deployment of MES (Manufacturing Execution System) solution including related business processes using the MES framework. - Design solutions for visualization of Manufacturing processes. - Digitalize Manufacturing processes to enhance standardization, transparency and controllability - Architecture and design of data systems for capturing and displaying of Manufacturing relevant information based on SAP ME/MII as well as its analysis and triggering the appropriate actions. - Definition and development of interfaces to manufacturing machines / equipment and manufacturing processes, interfaces from SAP ECC to SAP ME with business partners as well as their implementation. - Development of business processes in accordance to the standards of the quality system to ensure compliance. - Provide guidance on tools/system support for Operations including education and training materials. - Collaboration with the worldwide MES team. Qualifications Functional Skills Required: - Strong Solution Engineering Skills - Ability to understand complex business processes, convert into innovative solutions and fit into the overall Manufacturing system architecture - Programming experience in object-oriented languages (Java, .NET, C#) - Strong knowledge in the area of SAP ME/MII or other MES - Good knowledge in the area of SAP ECC (PP/MM) - Strong knowledge in the field of machine control and communication (PLC) - A systematic, target-oriented and independent method of working. - Demonstrate customer orientation and sense of urgency to all deliverables. - Excellent verbal and written communication skills required. Qualifications: - Bachelor or Masters degree in Engineering, Software Engineering or Computer Science discipline or equivalent - Project experience (typically 2-4 yrs) - Experience in implementing and supporting a MES - Manufacturing background with strong knowledge of shop floor processes - Experience with software validation would be helpful Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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27. OF & Supply Chain Manufacturing Test Tech – Wilmington, DE
Req ID: 2065858 Locations: Wilmington,Delaware,United States,Americas Relocation Benefits: NO Business: Agilent OF & Supply Chain Manufacturing Test Tech, (GC/MS) This position is required to support the manufacture of GCMS single quad instruments. This technician will be responsible for performing assembly/test and troubleshooting/repair of electronic assemblies to support production of the single quad product line. It will also include work on NPI products and close coordination with R&D development engineers. Specific responsibilities would include the following: - Execute routine and non-routine tests, troubleshooting, repair and quality verification of electronic modules, assemblies and boards used in GCMS instruments with limited technical support. - Perform complex test/process work requiring an in-depth technical background of GCMS instrumentation with limited documentation. - Support all other single quad production operations. - Assist engineering in developing new processes, test procedures, tools and prototype fabrication. - Independently monitors and adjusts process parameters, collects, manages and analyzes data and feedback, determines data collection needs and continuously improves processes, identifies root causes and drives the implementation of solutions. - Helps develop, suggest and implement process designs, program modifications, fixtures and works with mfg. eng. to implement them. - Proactively address customer or department needs and resolves problems. - May lead team efforts. - Reduce data to information (e.g. graphs, charts, including statistical analysis) and develop methods to apply the information and drive improvements. - Provide technical support for coworkers - Support team members in achieving the production line objectives and goals through effective teamwork. This includes providing constructive feedback to peers and maintaining flexibility to change on a daily basis. - This position will also include the coordination of some ESD responsibilities for the team. Physical Requirements This position will require the lifting of up to 40 lbs. multiple times per day/week. It may also require standing, sitting, stooping, bending for at least eight hours or more per day. Qualifications - AA/ AS degree in electronics with three years related experience OR equivalent combination of education and experience. - Demonstrated knowledge of GCMS - Demonstrated ability to apply analytical skills and understanding of the fundamentals involved in the product. (Physics, Chemistry, Electronics) - Demonstrated troubleshooting and "Diagnostic" and repair skills of assemblies to the component level. - Demonstrated ability to communicate both verbally and in writing. - Effective use of computer applications to perform work and special projects. - Demonstrated ability to read and understand product specification drawings and instructions. - Demonstrated willingness to take responsibility for resolving problems, and implementing new ideas or solutions. - Demonstrated use of tools and equipment to assemble small parts & high level of manual dexterity. - Demonstrated ability to utilize PC applications (e.g. SAP, Chemstation, Access, Excel) on a regular basis. - Demonstrated ability to read, understand and rigorously follow Quality System processes. - Demonstrated ability to adjust rapidly and effectively to change and remain open to new ideas and job assignments - Must have the ability to solder - Must be able to meet physical requirements Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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28. OF & Supply Chain Materials Procurement Associate – Sacramento, CA
Req ID: 2065788 Locations: Sacramento,California,United States,Americas Relocation Benefits: YES Business: Agilent OF & Supply Chain Materials Procurement Associate Agilent is seeking motivated individuals looking to develop skills in purchasing, supply-chain, quality, teamwork and communication. We have a great opportunity for someone to gain valuable experience working in procurement as a strategic buyer. The ideal candidate will have studied supply chain management and procurement. As a member of the Agilent Order Fulfillment & Supply Chain (OFS) team, the Supply Operations team member will: •Collaborate with stakeholders as the Supply Operations liaison, ensuring timely and effective day-to-day communication in areas such as production/planning priorities, material supply, problem resolution and escalations, as required. •Provide representation for Supply Operations in support of stakeholder requirements, utilizing Procurement knowledge & SAP skills. •Purchase critical/complex items to ensure availability of high-impact products. •Work with suppliers, negotiate pricing for products and/or services, coordinate and schedule delivery of materials. •Collaborate with suppliers to ensure optimal inventory levels to support on-time delivery. •Evaluate and select qualified suppliers based on competitive bids; lowest price, terms and conditions, quality, quantity, reliability, and ability to meet delivery schedules. •Monitor supplier performance; selecting/analyzing the supply base and developing and executing commodity plans. Qualifications Critical Skills & Behaviors: •Talent for establishing and maintaining positive work relationships. •Aptitude to follow verbal and written instructions with accuracy and strong attention to detail. •Effective verbal and written communication skills. •Effectively interacts and understands the different levels of the organization. •Seeks mutual agreement on expectations and deliverables; holds self and others accountable •Provides appropriate amount of communication to fit the situation. •Knowledge of appropriate software tools (e.g. SAP, Oracle, Nocturne, MS Office). •Possesses good general skills including time management, multi-tasking, flexibility, project management and prioritization. •Possesses continuous learning focus; takes initiative to continually expand knowledge base and return learning to the organization. •Owns personal development. •Embraces effective decision making skills; uses good judgment and can bring closure to issues. •Continually demonstrates reliability and delivery of measured results, which are executed with a sense of urgency. •Has a sensitivity for working with a culturally diverse workforce. •Demonstrates strong teamwork skills and is able to collaborate and work effectively with others, and to work independently. •Ability to work and manage multiple tasks in an interrupt driven environment. •Capability to adapt to changing priorities. •Willingness to work overtime as required. Desired: •Possesses knowledge of procurement and supply management practices. •Knowledge of appropriate systems (e.g. SAP, Oracle and web tools). Education Requirements: •Bachelors, Masters or University Degree in Supply Chain Management, Operations Management, Business or related field of study Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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29. OF & Supply Chain NPI Engineer – Lexington, MA
Req ID: 2066085 Locations: Lexington,Massachusetts,United States,Americas Relocation Benefits: YES Business: Agilent OF & Supply Chain NPI Engineer Primary Responsibilities: Participate as a team member of high caliber for Helium Leak Detector and Vacuum Product line. -Participates actively in new product introduction, including influencing the design of the product to ensure manufacturability and conformance with the global supply chain, enabling prototyping while in the R&D lab, testing the reliability of prototypes and managing the transition into production. -Supports and implements the transition of products and manufacturing processes from prototype to full production and through the entire life cycle of the product. -Improves products, processes and components to meet agreed-upon objectives. May involve redesign products or components to meet cost objectives, component technology obsolescence and customer requirements. Supports and implements the transition of products and manufacturing processes from prototype to full production and through the entire life cycle of the product. Work with Safety and Regulatory Lab to test and qualify existing or new product designs. Troubleshoot and make necessary improvements to ensure the product meets the necessary safety and EMC requirements. May direct the work of third party vendors and/or partners to meet contract specified deliverables, performance or business objectives Other Responsibilities: -Partners with procurement and technical services to improve/sustain products and processes. May direct the work of third party vendors and/or partners to meet contract specified deliverables, performance or business objectives. May work with suppliers to ensure achievement of goals for cost, quality and delivery of parts and materials. -May identify and manage ERP data such as bill of material and routing. - Work with manufacturing team to improve product yield, DeFOA and warranty failure rates. - May redesign or work with manufacturing team on to redesign products or components to meet cost objectives, component obsolescence and customer requirements. Performs qualification on prototype to characterize new design and ensure that it meets reliability and performance goals. May work with suppliers to ensure achievement of goals for cost, quality and delivery of parts and materials. Identifies and manage ERP data such as bill of material. Plans, evaluates and recommends technical, quality and cost specifications to meet design and business growth objectives and supply chain optimization. Identifies and qualifies alternative materials when needed. Work with manufacturing team to perform failure analysis for defect on arrivals and warranty failures and make the necessary improvements to enhance the quality and reliability of the product. Qualifications Qualifications: - Bachelors or University Degree or equivalent in Electrical, Electronics, or similar discipline. - Proactive team player who thrives on delivering solutions and results. - Excellent communication, collaboration and interpersonal skills. - Possess strong engineering and analytical skills. - Knowledge in basic statistical and quality tools knowledge. - Demonstrated knowledge in a variety of raw materials, metals, plastics is preferred. - Experience/ familiarity with vacuum technology or Helium Leak Detectors manufacturing process or equivalent in vacuum products will be an added advantage. - Willingness to work with team cross-geographical/different time zone is an added advantage Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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30. OF & Supply Chain Production Operator – Folsom, CA
Req ID: 2065717 Locations: Folsom,California,United States,Americas Relocation Benefits: NO Business: Agilent OF & Supply Chain Production Operator Want to join the growth engine of a Fortune 500 company in the life sciences and chemical analysis industry, and have a direct impact in a fast-paced supply chain? Agilent Technologies is seeking a technician for its growing consumables manufacturing facility located in the Sacramento, California region. Agilent’s laboratory consumables business is an industry leader in innovation, market share and performance. Agilent is seeking energetic, motivated individuals with demonstrated skills in quality, teamwork and communication. You'll set up and operate complex equipment and processes, manage multiple processes, establish objectives and implement improvements. This is an exciting opportunity to work in a fast-paced, high-throughput, leading-edge manufacturing facility, producing products used world-wide for ensuring quality and compliance in such areas as: consumer products, pharmaceuticals, drug testing, environmental monitoring, Homeland Security, forensics, and others. Qualifications The successful candidate will demonstrate the following: - Hands-on experience in a repetitive manufacturing environment - Strong attention to detail - Ability to see and work with small objects - Effective verbal and written communication skills - Aptitude to follow complex instructions - Capability to adapt to changing priorities - Skills in multi-tasking, planning, organizing workload and leading teams - Ability to work independently and within a team - Talent for establishing and maintaining positive work relationships - Willingness to work overtime as required - Ability to follow verbal and written instructions - Ability to handle small volumes of chemicals and solvents GEO Location: Folsom, CA. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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31. OF & Supply Chain Shipping Operator – Newport, DE
Req ID: 2066014 Locations: Newport,Delaware,United States,Americas Relocation Benefits: NO Business: Agilent OF & Supply Chain Shipping Operator - Second Shift Consider joining an exciting production team that provides consumables for Agilent's growing pharmaceutical and life sciences customer base. This position is located in Newport, Delaware. Relocation is NOT authorized. This is a second shift opportunity. Primary responsibilities include: - Pick, pack, troubleshoot, and process shipments in a timely manner - Maintain inventory of finished goods area - Order supplies as needed - Perform cycle counts - Maintain cleanliness and orderliness of work area - Contribute to the site's continuous improvement culture by developing and implementing ideas Other responsibilities include: - Provide back-up support to receiving, packaging, and kitting areas - Attend occasional meetings Follows all documented procedures and safety and environmental guidelines, and performs daily housekeeping duties. Performs other functions as requested by supervision. Mandatory overtime required at times. Agilent is a leader in life sciences, diagnostics and applied chemical markets. The company provides laboratories worldwide with instruments, services, consumables, applications and expertise, enabling customers to gain the insights they seek. Agilent’s expertise and trusted collaboration give them the highest confidence in our solutions. At our Delaware sites, located midway between Baltimore and Philadelphia, we have 800 people inventing, designing, building and marketing products that dominate the market for chemical analysis. Our products are frequently behind the headlines in the news, from environmental regulations to new drug discoveries to Homeland Security. You'll even see our instruments on television shows like "CSI". Qualifications May require some higher education or specialized training/certification. Requires a minimum of 3 years directly related experience, with typically 4 to 6 years' experience. Musts: - Demonstrated ability to work in a team environment. - Demonstrated strong communication and organizational skills. - Demonstrated ability to read and understand written procedures and instructions. - Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures). - Demonstrated ability to make timely decisions. - Demonstrated ability to maintain accurate records. - Experience working with computers: keyboarding, Windows environment, spreadsheets, word processing, databases. - Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach. - Required to remain standing for extended periods of time. - No known allergies to chemicals used in the work area. - Required to lift materials per entity specified and approved limits. - May be required to participate in medical/screening or monitoring programs. Desired: - Previous experience using SAP in a material coordination capacity. - Previous manufacturing experience in an ISO certified environment. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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32. Account Manager- Genomics (Alpharetta, GA)
Req ID: 2065567 Locations: Alpharetta,Georgia,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Account Manager- Genomics Join the Genomics team in Agilent's Life Sciences Group. The market for Agilent's Genomics products continues to enjoy significant growth through the invention, development and launch of high value products associated with technology platforms such as microarrays, Next Generation Sequencing, Quantitative PCR, synthetic biology, PCR and molecular biology reagents. In a direct sales role as a Genomics Account Manager, you will be responsible for driving sales of Agilent Technologies line of NGS (SureSelect and Haloplex), microarray, bioinformatics, synthetic biology, QC (Bioanalyzer & TapeStation), QPCR, and bioinformatics products within the territory. As an integral member of the field sales team you will use your excellent technical sales track record to focus on acquiring new customers while retaining and growing the existing installed base of customers. As a Genomics Account Manager, you will be expected to develop and implement successful strategies and tactics to sell complex Genomic solutions to high level contacts within this highly competitive marketplace. Key Responsibilities: •Driving sales of high performance Genomic products and services in a defined territory •Effectively prospect to find and close new opportunities in existing and new accounts. •Develop and maintain strategic buying relationships with customers and manage the overall relationship with accounts. •Conduct presentations and product usage demos with and without Field Application Engineer assistance. •Focus on strategic products applications (including targeted sequencing and custom expression) and solutions in strategic accounts •Contribute to developing effective strategies and tactics that will enable Agilent to gain market share. •Provide constructive feedback from customers into Agilent to help guide continual development of products that more effectively address customer needs. •Participate and be an active member in regional discussion groups and forums. •Understand Genomics in the Non-for-Profit and Pharmaceutical industry and recognize trends that impact buying of Agilent products •Represent Agilent to the customer AND the customer to the company. Qualifications •BS/MS in a Life Sciences discipline or Chemistry, or equivalent. •Solid self-management, organizational and prioritization skills •3+ years related direct life science product sales experience with a demonstrated track record of successfully selling against a quota. •Experience with NGS workflows, QPCR and DNA microarrays strongly desired. •Ability to work within a team selling environment. •Ability to interface at all levels within an organization for both internal/external customers. •Demonstrated commercial selling skills. Strong business development and sales closing skills. •Effective interpersonal communication and telephone sales skills. •Must be able to travel up to 25% of the time. Preferred location: Atlanta Georgia or Orlando Florida Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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33. Analytical Services Scientist – Boulder, CO
Req ID: 2065470 Locations: Boulder,Colorado,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Analytical Services Scientist •Outstanding communication skills, both written and oral, and will be expected to communicate directly with project managers and management. •Conducts method qualifications and validations per ICH Q2 and under current Good Manufacturing Practices (GMP) regulations and guidance per Food and Drug Administration (FDA) as well as International regulations. •Reviews data for compliance to specifications, and reports and troubleshoots abnormalities. •Helps Troubleshoot, investigate, and resolve analytical testing anomalies and drives solutions to improve the Quality Control program through effective corrective and preventive actions. •Ensures equipment is performing well and communicates and takes appropriate action as necessary. •Provides technical training on instrumentation •Required to follow good documentation practices. Qualifications Requires a degree in chemistry, biochemistry, or related field, and 5-7 years of related experience. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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34. Clinical Affairs Scientist – Carpinteria, CA
Req ID: 2065014 Locations: Carpinteria,California,United States,Americas Relocation Benefits: YES Business: Diagnostics and Genomics Group Clinical Affairs Scientist Dako North America, an Agilent Technologies Company Location: California (Carpinteria) We are searching for an experienced Clinical Affairs Scientist to work within the exciting field of oncology Companion Diagnostics (CDx). As a Clinical Affairs Scientist, your main responsibilities will be to determine clinical strategy in conjunction with team members, write clinical protocols, analyze data and write reports to support the clinical documentation of Companion Diagnostics (CDx)in the field of tissue-based Cancer Diagnostics. This position requires strong support to regulatory applications and scientific marketing activities. The top candidate will have a strong background in biostatistics and experience working in oncology drug, biomarker or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners,clinical and R&D scientists, Clinical Trial Managers and regulatory affairs to assure compliance with internal and external requirements. This position requires supervisory experience, overseeing a staff of 3-4 clinical affairs specialists. The successful candidate will be measured on: Your ability to contribute to the clinical strategy for CDx products. Your professional interactions and communication skills with pharmaceutical partners and regulatory bodies, such as the FDA. Your ability to work in a fast moving self-driven team. Your ability to write and interpret clinical protocols, reports and provide data analysis. Your ability to provide leadership and direction to the clinical affairs scientific staff. Qualifications University degree in pharmaceutical, medical or other relevant biological science, preferably, advanced degree. • Minimum 8 years experience in clinical studies for diagnostic, medical device or pharmaceutical products, including authoring protocols and reports. • A solid knowledge of clinical study design, biostatistics and Good Clinical Practice. • Knowledge of oncology and/or pathology is preferred. • Experience in working in parallel projects teams. • High work capacity may be required at certain times in high priority projects. • Experience from working with external international partners. • Advanced skills in both written and spoken communication. • Supervisory or management experience required. Geo Location: Carpinteria, CA Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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35. Clinical Affairs Specialist – Carpinteria, CA
Req ID: 2065378 Locations: Carpinteria,California,United States,Americas Relocation Benefits: YES Business: Diagnostics and Genomics Group Clinical Affairs Specialist We are looking for a Clinical Affairs Specialist to join Medical & Clinical Affairs at Dako. As a Clinical Affairs Specialist your main responsibilities will be to ensure clinical documentation for cancer in vitro diagnostics (IVDs), especially Companion Diagnostics (CDx), to support regulatory applications and scientific marketing activities. You will collaborate with statisticians to develop statistical plans, and work with investigators, internal R&D scientists, Clinical Trial Managers and RA/QA to assure compliance with internal and external requirements. You will be measured on: Your ability to contribute to the clinical strategy for CDx products. Your professional interactions and communication skills with pharmaceutical partners and internal cross-functional groups. Your ability to work in a fast moving self-driven team. Your ability to write author and interpret clinical protocols and data analysis. Responsible for scientific content of medical and clinical project deliverables, including scientific design and authoring of study protocols and reports. Develops and designs database and Data Report Forms. Conducts surveillance analysis in clinical trials. Responsible for the scientific validity of reported results and statistical analysis, tabulation and presentation of data. Authors Clinical Investigations section in Premarket Approval Applications, specific sections in Instructions for Use (IFU) and authors Performance testing Clinical section in 510(k) submissions. Prepares, revises and maintains procedures for the conduct of studies. Qualifications • University degree (PhD or MD required) in pharmaceutical, medical or other relevant biological science. • A minimum of 2-4 years experience of clinical studies for diagnostic, medical device or pharmaceutical products, including authoring protocols and reports. • A solid knowledge of study design, biostatistics and Good Clinical Practice. • Knowledge of oncology and/or pathology is preferred. • Experience in working in parallel projects teams. • High work capacity may be required at certain times in high priority projects. • Experience from working with external international partners. • Advanced communication skills, both written and spoken. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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36. Design Control Manager Research Associate – Carpinteria, CA
Req ID: 2065751 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Design Control Manager Research Associate, Companion Diagnostics Development Carpinteria CA We are currently seeking an experienced Research Associate with biological sciences background for our Dako North America office in Carpinteria, CA to work within the field of Companion Diagnostics. Job Summary Work in a dynamic environment in the field of Oncology: Plan and execute Design Control documentation strategies in support of teams working to develop Immunohistochemical Companion Diagnostic assays. Participate as key contributor in project teams by managing documentation packages and design reviews as required by Quality Management Systems. Facilitate transfer of completed development projects into products. Write/review packaging materials, improve established product reagents/protocols. Generate required documentation/procedures. Evaluate/optimize test methods and analysis of experimental results. Computer literate including Microsoft Word, Excel, and Outlook. Analytical, creative and works well in a team environment. Responsibilities: Create and maintain design control documentation in support of product development teams according to QMS procedures. Provide support to product development teams for Design Reviews and documentation according to QMS procedures. Work with the Design Control team to establish standardized best practices for Verification and Validation study design and documentation. Work with the Design Control team to identify and implement process improvements targeted toward time and cost efficiency. Participate in evaluating and reporting results including troubleshooting. Able to conduct internal and external presentations. General understanding of histology and pathology and ability to train others to follow design control procedures. Qualifications Education and/or Experience: BS or advanced degree in biological sciences Minimum 5 years relevant experience (product development/assay development/IHC/ISH). Industry experience preferred. Other Qualifications: •Good working knowledge of design control procedures and documentation requirements. •Good understanding of histology and pathology. •Demonstrated experience in cell biology methods such as immunohistochemistry, western blot, cell biology, flow cytometry •Broad base of general biology knowledge and laboratory experience •Able to organize and conduct internal presentations (external presentations desired but not required). •Ability to train others to follow design control procedures. •Mathematical (algebra and basic statistics) and computer (MS Office) skills Geo Location: Carpinteria, CA Agilent is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to disability, protected veteran status or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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37. Design Control Specialist Research Associate – Carpinteria, CA
Req ID: 2065627 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Design Control Specialist Research Associate, Companion Diagnostics Development Carpinteria CA We are currently seeking an experienced Research Associate with biological sciences background for our Dako North America office in Carpinteria, CA to work within the field of Companion Diagnostics. Job Summary Work in a dynamic environment in the field of Oncology: Plan and execute Design Control documentation strategies in support of teams working to develop Immunohistochemical Companion Diagnostic assays. Participate as key contributor in project teams by managing documentation packages and design reviews as required by Quality Management Systems. Facilitate transfer of completed development projects into products. Write/review packaging materials, improve established product reagents/protocols. Generate required documentation/procedures. Evaluate/optimize test methods and analysis of experimental results. Computer literate including Microsoft Word, Excel, and Outlook. Analytical, creative and works well in a team environment. Responsibilities: Create and maintain design control documentation in support of product development teams according to QMS procedures. Provide support to product development teams for Design Reviews and documentation according to QMS procedures. Work with the Design Control team to establish standardized best practices for Verification and Validation study design and documentation. Work with the Design Control team to identify and implement process improvements targeted toward time and cost efficiency. Participate in evaluating and reporting results including troubleshooting. Able to conduct internal and external presentations. General understanding of histology and pathology and ability to train others to follow design control procedures. Qualifications Education and/or Experience: BS or advanced degree in biological sciences Minimum 5 years relevant experience (product development/assay development/IHC/ISH). Industry experience preferred. Other Qualifications: •Good working knowledge of design control procedures and documentation requirements. •Good understanding of histology and pathology. •Demonstrated experience in cell biology methods such as immunohistochemistry, western blot, cell biology, flow cytometry •Broad base of general biology knowledge and laboratory experience •Able to organize and conduct internal presentations (external presentations desired but not required). •Ability to train others to follow assay protocols. •Mathematical (algebra and basic statistics) and computer (MS Office) skills Geo Location: Carpinteria, CA Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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38. Field Applications Scientist - Genomics Automation (Baltimore, MD)
Req ID: 2065624 Locations: Baltimore,Maryland,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Field Applications Scientist - Genomics Automation The Genomics business is seeking an enthusiastic, people-oriented, Pre/Post Sales Application Scientist to assist customers with our automated genomics workflows. The primary role of this position is to provide remote and onsite technical support for the Bravo NGS workstation. As the technical liaison between our customers and the field sales organization, you will be functioning in a pre-sales capacity by partnering with local sales staff to ensure automation solutions that customers are considering will meet their scientific needs. This may include evaluating the applications for automation feasibility, writing custom scripts/protocols using VWorks software as needed, and providing on-site automation training for new customers. In a post-sales technical role, you will be responsible for serving as the technical liaison between our sales organization, our customers, and our internal technical support channels to aide customers in troubleshooting and resolving technical issues that may arise. Other responsibilities for this position may include leading on-site instrument demonstrations with customer samples, representing Agilent at scientific conferences, and escalating issues other internal departments. You may also be asked to assist with the internal training of the sales organization and/or aide in the review/contribution to new application notes. Responsibilities include but are not limited to: • Co-traveling with sales representatives to customer labs to provide pre-sales technical consultation on Agilent’s automation solutions for the genomics business. • Performing product demonstrations in the field using customer samples. • Providing on-site application training at customer labs. • Demonstrating proper operating procedures with Agilent Genomics Solutions. • Reporting observations and sales opportunities to Product Marketing and Technical Support • Serve as a conduit between the online Technical Support team and Field Service Engineers • Develop custom scripts, in partnership with peers, to address customer-specific workflow needs Qualifications • BS/MS degree in molecular biology, genetics or similar field. PhD preferred. • Strong hands-on expertise with implementing automation solutions for genomics applications • Strong ability to troubleshoot molecular biology as well as hardware/automation repair • Laboratory experience with qPCR, PCR, and NGS strongly preferred • Industrial experience specifically providing pre/post technical support for a sales organization or providing technical seminars to an audience is a plus. • Excellent communication and teaching skills • Requires flexibility in working hours and available for >50% business travel. GEOGRAPHICAL LOCATION Must be based within the east coast corridor of the USA (ideally between Boston, MA and Baltimore, MD) Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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39. Immuno-Histo Chemistry Applications Specialist – Santa Clara, CA
Req ID: 2066078 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Immuno-Histo Chemistry Applications Specialist Are you looking to take your lab experience in Immuno-Histo Chemistry to the next level? To utilize your expertise to support the needs of our diverse internal and external customers in an exciting, dynamic role. Whether you are still working the bench or have since moved to other responsibilities, this exciting opportunity with Agilent will afford you the opportunity to capitalize on your experience and share your knowledge! Be a part of our growing internal education team where your technical and scientific expertise can be leveraged. Agilent is a leader in life sciences, diagnostics and applied chemical markets. We provide laboratories worldwide with instruments, services, consumables, applications and expertise, enabling customers to gain the insights they seek. Agilent gives doctors a head start in the fight against cancer and other diseases. Our solutions help pathology laboratories deliver fast, accurate information and help medical professionals make more precise diagnoses so patients can receive the most effective therapies. As an Immuno-Histo Chemistry Applications Specialist, your responsibilities will include acting as a subject matter expert for our internal staff and external customers. Responsibilities would include the delivery of instruction, mentoring and support from both an educational and technical perspective; assisting in translating customer's educational requirements into single seminars, customized solutions or projects, which improve the effectiveness and intellectual capital for our customers. Will also work with customers and internal organizations to develop specifications, and design and conduct technical training courses for customers and/or employees. Other tasks/ responsibilities may include: • Leading participants in classroom lectures and/or laboratory training sessions. • Providing support through technical communication with internal staff, field based representatives, customers and end users. • Assist in developing new and novel methods of teaching relevant industry topics. • Utilizing internal systems to place orders for regents, tissue and other supplies necessary to perform tasks. Qualifications • 5+ years relevant experience including hands on laboratory experience and strong pathology, technical, and instrument background. • Post Graduate, Masters Degree, Bachelors Degree and/or equivalent combination of education and experience. • Lab based Cytotechnologist or Histotechnologist experience. • ASCP certification preferred but not required. • Out of box thinker who can provide alternative ways to communicate a process • Ability to effectively interact with a diverse group of people including various skill levels, degrees of seniority, personality, appreciation for the topic, and ego. • Prior training and/or experience in automation focused ImmunoHisto Chemistry and In Situ Hybridization markets; including special stains and hematoxylin and Eosin preferred. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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40. Chemist – Boulder, CO
Req ID: 2065967 Locations: Boulder,Colorado,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Manufacturing Chemist Agilent Technologies Life Sciences Chemical Analysis business is looking to add a Manufacturing Chemist to their high-performance manufacturing team working at the state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Boulder, Colorado. Key responsibilities include: - Actively involved in the manufacturing of oligonucleotide APIs in a GMP environment. - Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing. - Occasionally writing standard operating procedures according to regulatory and procedural guidelines. - Working with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.). - Maintaining, calibrating, and trouble shooting critical process equipment. Qualifications • BS in chemistry, biology, biochemistry, science or equivalent and/or a combination of equivalent education and or experience • 5 to 8 years of related experience in a pharmaceutical manufacturing environment preferred • Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is advantageous. • Detail oriented and can perform technical duties following standard operating procedures and general laboratory safety rules. • Ability to work both independently and in a team setting on a variety of projects and use individual discretion to meet required project objectives and deadlines. • Excellent math, documentation, communication and operational trouble shooting skills. • Mechanically inclined. • Ability to work as a successful member of a team working to establish priorities, scheduling, and procedures that collectively will meet department goals and project deadlines. • Ability to work in a clean room environment. • Previous experience in a FDA regulated manufacturing environment highly desired Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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41. Materials Coordinator – Boulder, CO
Req ID: 2065769 Locations: Boulder,Colorado,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Materials Coordinator Agilent Technologies Life Sciences Chemical Analysis business is looking to add a Material Coordinator to their high-performance Supply Chain team working at the state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Boulder, Colorado. Duties and Responsibilities include the following: • Assembles, stages, and transfers the materials needed for a production operation from the warehouse to manufacturing in accordance to the production schedule. Responsible to work directly with sourcing, material planning and manufacturing personnel to ensure the necessary materials and quantities are transferred and available for production operations. • Reconciles materials following production operations. Electronically and physically ensures remaining materials are returned from manufacturing to warehouse storage locations. • Maintains inventory control by ensuring that all material movements (warehouse to manufacturing, manufacturing to warehouse, etc.) are properly reflected in SysPro. • Maintains inventory accuracy by ensuring material used in manufacturing is accurately reflected in SysPro. Reconciles inventory discrepancies between the physical stock and SysPro. • Safeguard inventory levels by notifying planning, logistic and procurement personnel when materials are observed to be near or below the minimum stock level. • Performs general departmental duties such as conducting inventory counts, removing retest or expired materials from manufacturing, maintaining inventory levels and other general inventory tasks. Qualifications Bachelor's degree and three years related experience preferred and/or equivalent combination of education and experience. Training in cGMP regulated facility in the biotech, pharmaceutical or chemical industry strongly preferred. Experience working in fine chemicals or pharmaceutical manufacturing in addition to: • Proficient with Microsoft Office software and Enterprise Resource Planning (ERP) management systems (i.e. Syspro). • Knowledge and adherence to cGMP and international regulations (i.e. ICH Q7) pertaining to the production of APIs. Ability to consistently follow Standard Operating Procedures (SOPs) and site policies. • Ability to read and understand the material information specified and documented in batch records and solution preparation forms. • Ability to operate fork lift, pallet jack and other powered material handling equipment. • Ability to author and revise SOPs, forms and reports as needed. • Ability to manage multiple simultaneous projects and priorities. Ability to prioritize projects and establish short and long-term plans to complete projects according to schedule. • Ability to work collaboratively as a team to meet project deadlines and objectives, yet make independent decisions on various tasks. • Skill in effective communication, both written and verbal. Ability to effectively present information to and respond to questions from internal clients, managers, and contractors. • Knowledge and adherence to OSHA, hazardous materials and local safety guidelines. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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42. Product Manager- Cytogenetics – Santa Clara, CA
Req ID: 2066077 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Product Manager- Cytogenetics Agilent’s Diagnostics & Genomics Division has a history of developing high-quality, vibrant, and profitable product offerings, and we are looking for a Product Manager / Senior Product Manager to join our high-performance Human & Reproductive Genetics Team. The Product Manager – Cytogenetics will be responsible for managing our market-leading chromosomal microarray product portfolio with a focus on development and execution of strategies to continue to grow Agilent’s successful microarray business in the clinical cytogenetics market space. Key Responsibilities: -Strategically evaluate new product opportunities and identify synergies with other Agilent products. - Develop and execute portfolio product marketing strategies to achieve stated revenue, profitability and market share objectives. -Develop novel product launch strategies and implement launch plans. -Define pricing strategy, product positioning and configuration to ensure the best possible performance versus business goals. -Set product-pricing strategies including discount structures, and manage those strategies in conjunction with market dynamics and target markets. -Collaborate with cross-functional partners from other Agilent groups including marketing from other business units, R&D, manufacturing, and sales to achieve business objectives. - Work with KOLs to drive market penetration in specific application areas including prenatal, postnatal, and IVF. - Work with the Launch Excellence Team to develop programs and collateral material for New Product Introductions and for on-market products. - Define training and content requirements for products and programs. - Drive the product/marketing message through all communication channels. - Participate in key sales situations for the product. Qualifications - BS in biology, biochemistry, molecular biology; related discipline or equivalent. - 6+ years’ experience in marketing life science or diagnostic products, with at least 3 years of Product Management experience as well as cytogenetic experience in career history. - Experience in molecular diagnostics or regulated environments. - The ideal candidate will bring a very strong cytogenetics background to the table; experience with aCGH products is a plus. - Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success. - Strong advocate for customer-driven product development. - Demonstrate ability to develop marketing plans that align with strategic objectives. - Ability to work independently; to plan, prioritize workload, schedule time, assess and solve problems. - High proficiency in pricing and forecasting. - Must exhibit strategic thinking, teamwork, creativity, planning and organization, and flexibility. - Strong analytical and decision making skills. - Experience in working with global markets/customers. - Excellent written and oral communications skills and comfortable presenting to high level audiences both internally and externally. - Must have flexibility in working hours and available for 25% business travel. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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43. Product Manager, Synthetic Biology Products – Santa Clara, CA
Req ID: 2064997 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Product Manager, Synthetic Biology Products Come join the fast-moving and exciting Genomics business at Agilent Technologies. We have a great group of talented individuals in an environment of market-leading products and enabling technologies along with a healthy R&D roadmap for the right Marketing professional to thrive in. This position will manage an exciting area of growth in Synthetic Biology products for Agilent. Your skills in product management, in-depth knowledge of genomic technology and strong understanding of biological research will enable you to play a key role in the development and marketing of these products for the Agilent Genomics Business' Molecular and Synthetic Biology Solutions team. We are seeking a highly skilled and very energetic Product Manager to work closely with R&D, Sales, and customers to develop and prioritize product requirements, enhancements, and new product offerings to enable customers to be successful in their incorporation of molecular and synthetic biology tools into complex genome engineering workflows. The ideal candidate will possess a broad understanding of genomics/genetics, genome engineering, synthetic biology, and have superior leadership and cross-functional communication skills to be able to successfully manage complex projects and influence multi-disciplinary teams. The candidate should have a high level of business acumen which will be leveraged in both the development of strong business cases for the development of new products, as well as rationalizing the commercial life cycle of products from launch to obsolescence. Responsibilities: • Develop, refine and communicate product requirements, plans and specifications based on first-hand knowledge of molecular and synthetic biology tools and customer requirements. • Interface with R&D to translate and prioritize customer requirements into specific bioinformatics software requirements. • Develop detailed market and customer requirement documents and resulting product roadmap plans. Communicate and implement product plans working closely with marketing, R&D, and manufacturing. • Develop powerful and targeted marketing collateral in partnership with Marketing Programs and Field Marketing teams to help drive sales of current portfolio as well as new products • Keep abreast of market and technical trends, competitor products and customer requirements to determine competitive strategies for current and future products. • Establish relationships with key customers and provide feedback on product offerings. • Approximately 25% travel will be required. • Foster a strong working relationship with global sales, partnering effectively to answer questions regarding product offering to drive product sales to achieve growth objectives. Qualifications • Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline required. MS or PhD preferred. MBA a plus. • 5+ years of sales or marketing experience in Genomics or related field. • Ability to communicate and discuss molecular biology applications in cloning, mutagenesis and genome engineering with internal R&D scientists and customers. • Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization. • Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success. • Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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44. Project Manager, Companion Diagnostics – Carpinteria, CA
Req ID: 2065626 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Project Manager, Companion Diagnostics Agilent Technologies Diagnostics and Genomics Group (DGG) is seeking an experienced PROJECT MANAGER, with pharmaceutical / diagnostics background, to lead project core teams focused on the development of companion in vitro diagnostics products (pharmDx) in an exciting, challenging and collaborative environment. You will have the opportunity to take your PROJECT MANAGEMENT expertise to a new level managing Agilent’s COMPANION DIAGNOSTIC project teams. You will be a key player for a company that is leading the way in COMPANION DIAGNOSTIC product development. Your role in this position will be externally facing to pharmaceutical industry partners, and responsible for planning, directing and executing designated projects between DGG and its pharma partners. The successful person for this job will work closely with global cross-functional project teams, line management and external partners to ensure that objectives of projects are accomplished within prescribed time frame and within budget. Responsibilities include: • Leading global cross-functional COMPANION DIAGNOSTICS project teams, and serving as a direct contact between pharma project managers and key DGG stakeholders • Leading, driving and delivering expected results according to agreed project scope, cost, quality and timeline milestones • Creating and managing resource forecast plans, and working directly with line managers to communicate and agree to project staffing requirements • Tracking projected project revenues, costs, expenses and profits against defined metrics; proactively communicating deviations to relevant stakeholders • Analyzing, planning and tracking project phases and activities, and communicating the timelines/milestones/goals on a regular basis to DGG management, the project team and other stakeholders • Effectively identifying and communicating risks to stakeholders in a timely and clear fashion • Re-evaluating goals throughout the project, together with the project’s stakeholders, and making necessary adjustments to project plans and budgets • Participating in preparation and alignment of decision process in joint project governance bodies • Establishing and maintaining project lifecycle documentation • Mentoring of project team members in Agilent business and quality practices Required skills: • Ability to work collaboratively with external customers to insure that company and partner interests are addressed in a balanced fashion • Ability to manage global, multi-site teams including direct and indirect project resources • Ability to establish trust and work with integrity while motivating others to achieve the goals of the project • Proven leadership and desire to succeed with a minimum level of guidance, while successfully multi-tasking amongst several competing initiatives • Excellent presentation skills • Creative problem solving skills and decision making abilities that adapt to change and promote teamwork across geographies and cultures • Ability to influence internal and external stakeholders at all levels in a matrixed team environment • Experienced in constructive decision making, resolution of conflict, and the building of effective top-down and bottom-up business relationships • Active ownership of problems of diverse technical and business scope where the analysis requires in-depth evaluation and research of competing options • Understanding of the proper application of risk management techniques to ensure business priorities and quality standards are met
• Ability to adapt to new technologies and scientific disciplines while ensuring consistent application of lifecycle management processes across domains Qualifications • B.S. or B.A. in Science, Engineering, or Project Management with an understanding of the biological sciences; PMP certification a plus • Minimum of 3 years of relevant experience managing complex development projects in the pharmaceutical or diagnostics market • Strong analytical skills with a proven ability to balance and prioritize responsibilities in accordance with business and team needs • Experience defining and maintaining strategic direction while ensuring successful execution of project details • Demonstrated exceptional interpersonal and communication skills with the ability to effectively communicate with individuals at all levels in the organization across various functions (research, development, manufacturing, quality control, marketing) and locations • Established expertise and hands-on experience with Microsoft Project, Word, Excel, PowerPoint, Outlook, Sharepoint and remote meeting tools such as WebEx, Live Meeting, etc. • Excellent time management skills and ability to work independently • Strong business acumen, negotiation and delegation skills, and ability to influence at all levels within the organization. • Ability to travel, up to 30 travel days a year, both domestic and international. Geo Location: Carpinteria, CA Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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45. Project Manager, Companion Diagnostics – Carpinteria, CA
Req ID: 2065802 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Project Manager, Companion Diagnostics Agilent Technologies Diagnostics and Genomics Group (DGG) is seeking an experienced project manager, with pharmaceutical / diagnostics background, to lead project core teams focused on the development of companion in vitro diagnostics products (pharmDx) in an exciting, challenging and collaborative environment. You will have the opportunity to take your project management expertise to a new level managing Agilent’s companion diagnostic project teams. You will be a key player for a company that is leading the way in companion diagnostic product development. Your role in this position will be externally facing to pharmaceutical industry partners, and responsible for planning, directing and executing designated projects between DGG and its pharma partners. The successful person for this job will work closely with global cross-functional project teams, line management and external partners to ensure that objectives of projects are accomplished within prescribed time frame and within budget. Responsibilities include: • Leading global cross-functional Companion Diagnostics project teams, and serving as a direct contact between pharma project managers and key DGG stakeholders • Leading, driving and delivering expected results according to agreed project scope, cost, quality and timeline milestones • Creating and managing resource forecast plans, and working directly with line managers to communicate and agree to project staffing requirements • Tracking projected project revenues, costs, expenses and profits against defined metrics; proactively communicating deviations to relevant stakeholders • Analyzing, planning and tracking project phases and activities, and communicating the timelines/milestones/goals on a regular basis to DGG management, the project team and other stakeholders • Effectively identifying and communicating risks to stakeholders in a timely and clear fashion • Re-evaluating goals throughout the project, together with the project’s stakeholders, and making necessary adjustments to project plans and budgets • Participating in preparation and alignment of decision process in joint project governance bodies • Establishing and maintaining project lifecycle documentation • Mentoring of project team members in Agilent business and quality practices Required skills: • Ability to work collaboratively with external customers to insure that company and partner interests are addressed in a balanced fashion • Ability to manage global, multi-site teams including direct and indirect project resources • Ability to establish trust and work with integrity while motivating others to achieve the goals of the project • Proven leadership and desire to succeed with a minimum level of guidance, while successfully multi-tasking amongst several competing initiatives • Excellent presentation skills • Creative problem solving skills and decision making abilities that adapt to change and promote teamwork across geographies and cultures • Ability to influence internal and external stakeholders at all levels in a matrixed team environment • Experienced in constructive decision making, resolution of conflict, and the building of effective top-down and bottom-up business relationships • Active ownership of problems of diverse technical and business scope where the analysis requires in-depth evaluation and research of competing options • Understanding of the proper application of risk management techniques to ensure business priorities and quality standards are met • Ability to adapt to new technologies and scientific disciplines while ensuring consistent application of lifecycle
management processes across domains Qualifications • Minimum of 5-7 years of relevant experience managing complex development projects in the pharmaceutical or diagnostics market • Strong analytical skills with a proven ability to balance and prioritize responsibilities in accordance with business and team needs • Experience defining and maintaining strategic direction while ensuring successful execution of project details • Demonstrated exceptional interpersonal and communication skills with the ability to effectively communicate with individuals at all levels in the organization across various functions (research, development, manufacturing, quality control, marketing) and locations • Established expertise and hands-on experience with Microsoft Project, Word, Excel, PowerPoint, Outlook, Sharepoint and remote meeting tools such as WebEx, Live Meeting, etc. • Excellent time management skills and ability to work independently • Strong business acumen, negotiation and delegation skills, and ability to influence at all levels within the organization. • Ability to travel, up to 30 travel days a year, both domestic and international. • B.S. or B.A. in Science, Engineering, or Project Management with an understanding of the biological sciences; PMP certification a plus GEO Location: Carpinteria, California Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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46. Quality Engineer - New Product Introductions – Santa Clara, CA
Req ID: 2065472 Locations: Santa Clara,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Quality Engineer - New Product Introductions Job Duties: • Serve as the quality representative for new product introduction and new product improvement projects for all product types; participate in team meetings and coordinate quality activities as required • Assist with the verification and validation experimental design; coordinate with regulatory affairs and R&D to confirm experimental design conforms to appropriate regulatory requirements • Create and/or update design and process FMEA • Review, create, and/or update traceability matrices • Conduct detailed reviews of all design history files; coordinate with project management, R&D, and manufacturing as needed ensure the project deliverables are complete, accurate, and in compliance with regulatory requirements • Coordinate efforts associated with the preparation of regulatory documents or submissions in a timely manner to facilitate worldwide product launches • Assess and update design and quality process documentation as required to elevate existing Research Use Only (RUO) products to Class I Clinical Laboratory Instruments, Software, General Purpose Reagents and/or CE-IVD regulations • Identify gaps and update Design History Folders (DHF) and Device Master Records (DMR) for the existing products • Identify gaps in design verification and validation and update them to meet the requirements of Class I and/or II medical devices • Create and/or update technical files • As needed, coordinate with production manufacturing to bring device master record documentation to QSR levels Qualifications Qualifications: • Bachelors or Master's Degree or equivalent in Biological science or equivalent • 5+ years of experience in a biological manufacturing environment. Must have prior experience with wet lab bench work. Prior experience with next generation sequencing is preferred • Must have 3+ years of hands on experience writing and executing validation protocols and reports for the medical device industry • Must have experience in ISO13485 or quality environment supporting clinical markets • Understanding of how to work quickly in a regulated environment establishing processes for integration of revision control, validation, and implementation of changes • Experience with bioinformatics and statistical design is greatly preferred • Proficient in Microsoft office suite required. Experience using bioinformatics data analysis software is preferred Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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47. Regulatory Affairs Specialist – Carpinteria, CA
Req ID: 2064738 Locations: Carpinteria,California,United States,Americas Relocation Benefits: YES Business: Diagnostics and Genomics Group Regulatory Affairs Specialist Dako North America, an Agilent Technologies Company Location: California (Carpinteria) We are searching for an experienced regulatory professional to work within the Companion Diagnostics (CDx) team of Dako North America, an Agilent Technologies company. Reporting to the Sr. Director, Regulatory Affairs (CDx), the successful candidate must have global regulatory experience working in IVD, Medical Devices or Pharmaceutical, with a history of successful regulatory submissions, registrations, 510(k)’s and PMA approvals in US and Asia. The prefered candidate has experience in Companion Diagnostics, and has lead company-sponsored interactions with regulatory bodies, especially FDA. The candidate must have excellent oral and written communication skills. The candidate will represent Regulatory Affairs on project teams and in close collaboration with pharmaceutical partners. Responsibilities 1) Provide expertise in regulatory affairs leading to the successful regulatory registrations and approvals of Companion Diagnostic products in global markets. 2) With Regulatory Sr. Management, develops regulatory strategies related to CDx product development. 3) Provides regulatory assessments and plans for international product registrations and approvals. 4)Interacts and collaborates with pharmaceutical partners in joint meetings. 5)Ensures the accurate and timely preparation of regulatory submissions and reporting in accordance with Company goals, regulatory requirements and partnership contracts. 6)Works across the Agilent organization to ensure alignment of regulatory processes, standards and compliance. Provide expertise and advice in obtaining CDx product registrations and approvals in the Pacific Asian market. 7) Represents the Company in 3rd party meetings, especially the FDA, and regulatory associations. 8) Stays abreast of global IVD regulations and guidances, especially those relevant to Companion Diagnostics. Qualifications Bachelors or Masters Degree or University Degree or equivalent. 5-6 years relevant experience Post-graduate and/or certification/ license may be required. Requires specialized depth and/or breadth of expertise in job. Geo Location: Carpinteria, CA Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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48. Research Assistant, Companion Diagnostics – Carpinteria, CA
Req ID: 2065210 Locations: Carpinteria,California,United States,Americas Relocation Benefits: YES Business: Diagnostics and Genomics Group Research Assistant, Companion Diagnostics We are currently seeking a Research Assistant with a biological sciences and histology background for our Dako North America office in Carpinteria, CA to work within the field of Companion Diagnostics. Job Summary: Under supervision perform experiments to develop and validate immunohistochemical (IHC) assays in the pharmDx business area. Participate as contributor on cross-disciplinary project teams. Facilitate transfer of completed development projects into products. Contribute to study protocols, technical reports, and packaging materials. Maintain a laboratory notebook, provide customers and co-workers with technical support. Computer literate including Microsoft Word, Excel, and Outlook. Works well in a team environment. Responsibilities: •Perform studies as described and detailed in existing documents. •Execute performance testing of companion diagnostic IHC assays. •Support clinical trial activities, including preparation of study materials and support of training of study personnel. •Participate in evaluating and reporting experimental results. •Contribute to generation of protocols and reports. •With training and coaching, gain understanding of histology and pathology, especially with regard to oncology and cancer biomarkers. Qualifications Education and/or Experience: •B.S. in the biological sciences (or equivalent in work experience). •0-2 years relevant experience. Other Qualifications: •Able to follow Quality System regulations, including Design Control. •Experience in a biology laboratory setting is highly desirable. •Experience with immunohistochemical staining and use of a microscope preferred. •Works well in a team environment. •Proficient with Microsoft Office. We offer: A challenging job at an dynamic international company, working with one of the most rapidly growing areas in the biopharmaceutical industry. You will become part of company that works according to these values: •We care about the needs of our customers and cancer patients and strive to ensure people are treated consistently, fairly and with respect. •We deliver effective diagnostic solutions valued by our customers. •We are passionate about quality in the solutions we provide to our customers, in the talented people we attract and develop. Location: Carpinteria, CA Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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49. Research Assistant, Companion Diagnostics – Carpinteria, CA
Req ID: 2066113 Locations: Carpinteria,California,United States,Americas Relocation Benefits: NO Business: Diagnostics and Genomics Group Research Assistant, Companion Diagnostics We are currently seeking a Research Assistant with biological sciences background for our Dako North America office in Carpinteria, CA to work within the field of Companion Diagnostics (pharmDx). Job Summary Work in a dynamic environment in the field of Oncology! Under appropriate guidance, plan and execute experiments to develop immunohistochemistry (IHC) assays in the Companion Diagnostics business area. Participate as key contributor in project teams. Facilitate transfer of completed development projects into commercial products. Contribute to improvement of established product reagents/protocols. Contribute to generation of required documentation/procedures. Evaluate/optimize test methods, new antibodies/reagents. The ideal candidate will be an enthusiastic, friendly, flexible team member who learns quickly, enjoys multi-tasking, and most important, has an interest in the company and our products. Dako promotes a mutually respectful environment where all staff members are essential for the success of the group. Responsibilities: Perform studies as described and detailed in existing documents. Execute performance testing of companion diagnostic IHC assays. Support clinical trial activities, including preparation of study materials and training of study personnel. Participate in evaluating and reporting experimental results. Contribute to generation of general protocols and reports (Stability; short Tech Reports etc) and publications. With training and coaching, increase understanding of histology and pathology, especially with regard to Oncology and relevant Biomarkers. Participate in product care activities as needed. Qualifications Education: Bachelors degree in the biological or chemical sciences or equivalent in work experience. Years of Experience: 0-2 years with Bachelors degree or related experience Other Qualifications: Able to follow Quality System regulations, including Design Control. Experience with high throughput digital whole slide scanning and image analysis is highly desirable. Experience with immunohistochemical staining and use of a microscope preferred. Good verbal and written communications. Analytical, creative and works well in a team environment. Proficient with Microsoft Office. Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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50. Research Associate- Histologist – Carpinteria, CA
Req ID: 2065141 Locations: Carpinteria,California,United States,Americas Relocation Benefits: YES Business: Diagnostics and Genomics Group Research Associate- Histologist Histologist, Companion Diagnostics Dako North America Carpinteria, CA This position requires the ability to document testing parameters and results, follow protocols, procedures and specification to generate quality product. Responsibilities: Must me familiar and understand tissue procurement regulations including HIPAA and informed consent, activities associated with generating and completing data and work orders contained in the Tissue Inventory Program (TIP), microtomy; embedding, tissue fixation/processing and staining procedures (H&E/special stains/IHC/ISH). These tasks may be accomplished by using various forms of histology equipment such as: microtome, cryostat, automated tissue processor, TMA instrument and automated IHC stainer. The Histologist must be able to perform all tasks with consistent quality results, adhering to established laboratory policies/guidelines while maintaining a safe working environment. This position will require accurate document recording to comply with various internal and external regulations. The Histologist will assist in routine preventative maintenance/cleaning, coordinating preventive and corrective maintenance of histology laboratory equipment & instruments and also be required to assist in overseeing the implementation, validation and evaluation of new equipment used in the histology laboratory. A complete knowledge and understanding of Histology equipment function is required. Supervisory Responsibilities: This position has no supervisory responsibilities Qualifications 3+ years experience as a histologist in a clinical or research laboratory. ASCP certified Histology technician or technologist is desired. •Bachelor’s degree in Biological Science, Basic Science and/or ASCP certification as a Histology Technician or Technologist. Histology experience in a clinical or reference lab. Alternatively, education and training as a medical transcriptionist, coupled with experience in a Pathology laboratory environment. •Knowledge of Pathology nomenclature. •Attention to details and works to complete all tasks in an organized manner. •Extensive exposure to pathology tissue/disease nomenclature. •Capability of performing multiple tasks simultaneously and accurately. Able to quickly adjust to changing workloads and priorities. •Working knowledge of OSHA requirements concerning chemical hygiene, biohazards and blood-borne pathogens. Demonstrated capability of safely handling carcinogenic substances, odorous and other hazardous materials/reagents. •Good written and verbal communication. •Working knowledge of Microsoft Office and familiarity with Oracle and or Agile or other inventory control and document change systems is preferred. Skills: Microtomy, embedding, H&E staining, tissue fixation/processing and grossing. Analytical techniques, Immunohistochemical techniques, Good Laboratory Practices (GLP) and Standard Operating Procedures (SOP’s). Basic computer skills including familiarity with Microsoft Office Suite. Geo Location: Carpinteria, CA Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Please have all applicants apply at www.jobs.agilent.com
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