Sr. Scientist (R2-R3)
About The Position
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Eli Lilly and Company seeks a Sr. Scientist (R2-R3) to provide technical support for the manufacturing of Active Pharmaceutical Ingredients (APIs). Support the technology transfer and process validation of manufacturing processes in external manufacturing area. Execute technical projects to improve and optimize process control, yield, purity, and productivity. Perform process monitoring on the manufacturing data to assess process variability and identify process improvement opportunities. Author and review technical documents to translate process knowledge and control strategies into manufacturing documentation. Serve as the frontline technical services and active member of process teams to achieve project and manufacturing goals.
Requirements
- Bachelor’s degree in Chemical Engineering, Biochemistry, Physical Chemistry or a related STEM field
- 3 years of experience in GMP API manufacturing from TS/MS or Development organization
- 3 years of experience in cGMP manufacturing
- 3 years of experience in small molecule API Manufacturing
- 2 years of experience in process scale up
- 2 years of experience in pilot plant pharmaceutical manufacturing
- 2 years of experience in technology transfer of small molecule synthetic drug substance
- 2 years of experience in process validation and data monitoring
- 1 year of experience in root cause analysis investigation at cGMP setting
Responsibilities
- Provide technical support for the manufacturing of Active Pharmaceutical Ingredients (APIs).
- Support the technology transfer and process validation of manufacturing processes in external manufacturing area.
- Execute technical projects to improve and optimize process control, yield, purity, and productivity.
- Perform process monitoring on the manufacturing data to assess process variability and identify process improvement opportunities.
- Author and review technical documents to translate process knowledge and control strategies into manufacturing documentation.
- Serve as the frontline technical services and active member of process teams to achieve project and manufacturing goals.
Benefits
- company bonus (depending, in part, on company and individual performance)
- company-sponsored 401(k)
- pension
- vacation benefits
- medical benefits
- dental benefits
- vision benefits
- prescription drug benefits
- flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
- life insurance
- death benefits
- certain time off and leave of absence benefits
- well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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What This Job Offers
Job Type
Full-time
Career Level
Senior
