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Senior associate-quality control

Liverpool (Merseyside)
Elanco
Quality controller
Posted: 29 January
Offer description

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your role:

This is a laboratory-based position within the Analytical Service Centre (ASC) laboratory. The role involves the execution of the analytical work required for the characterization of the Elanco reference standard portfolio. This will include some analytical method development, fit for purpose method qualification/validation, execution of compendial and non-compendial test methods, solution stability studies and generation of other analytical data as needed. In addition, the role also includes analytical method remediation/improvements, validation and transfer supporting manufacturing / customer supply, commercialisation, quality and regulatory aspects of the business.

Your responsibilities:

1. Perform reference standard characterization testing using a variety of analytical techniques (IR, HPLC/UPLC, KF, NMR) documenting results in GMP compliant reports
2. Use appropriate scheduling and planning to ensure reference standard work is executed within agreed timelines
3. Performing analyses and appropriately documenting results to support method remediation and method verifications/validations/transfers to GMP standards.
4. Employ good GMP documentation practices to thoroughly and accurately document all work in a timely manner
5. Use problem solving/troubleshooting skills to investigate laboratory issues and identify root causes
6. Execute and document laboratory investigations, deviations and change controls using an electronic Quality Management System (Veeva)
7. Maintain laboratory and office areas in compliance with EHS and cGMP requirements.
8. Perform all aspects of Sample/Ref Std handling, eg receipt, storage and disposal as per procedures.
9. Conduct laboratory equipment calibrations and maintenance.
10. Write, update and review SOPs, validation protocols and reports
11. Follow lab purchasing procedures to ensure laboratory remains sufficiently stocked with standards/reagents and consumables.
12. Complete all mandatory training within expected timelines and ensure you are trained before performing any laboratory task.
13. Communicate with internal and external auditors (eg Elanco corporate auditors, FDA, VMD, etc) in accordance with company policy and procedures.

What You Need to Succeed (minimum qualifications):

14. BSc or equivalent in a relevant Chemistry discipline
15. Strong working knowledge of GMP analytical laboratory operations achieved by at least 5 years experience of working in such an environment
16. 5-10 years of practical experience of HPLC analysis in a GMP Lab
17. Experience in performing GC, IR and Karl Fisher analyses
18. Ability to work collaboratively as well as independently to achieve goals
19. Self starter with excellent written and verbal communication

What will give you a competitive edge (preferred qualifications):

20. Previous experience of using Waters integration package (Empower)
21. Previous experience of using an electronic document management system
22. Practical experience of executing method validations (especially for LC methods)
23. Analyses using Nuclear Magnetic Resonance (NMR) equipment
24. Dissolution Testing

Additional Information:

25. Work schedule 7:30 hour days Monday to Friday on site

Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

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