Scientist - TS/MS Parenteral - Visual Inspection
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.
Requirements
- Bachelor's degree or higher in an engineering, science, or related field.
- Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
Nice To Haves
- Pharmaceutical and/or medical device manufacturing experience.
- Root Cause Investigation Experience.
- Proficiency with computer systems including Microsoft Office products, Veeva Vault, TrackWise, electronic batch records, and SAP.
- Demonstrated successful leadership of cross-functional teams.
- Strong interpersonal and teamwork skills.
- Strong self-management and organizational skills.
Responsibilities
- Support the assigned Process Team (formulation, filling, or VI) as TSMS representative.
- Serve as floor-level support and technical interface for manufacturing components, equipment, and operations for the TSMS team.
- Represent Concord TSMS team for internal and external communications on a regular basis.
- Lead risk management activities as it pertains to product/process.
- Provide technical support to non-routine (e.g., deviation, complaint) investigations, including consultation on quality and stability issues.
- Prepare and Review or approve, as required, relevant technical documents such as: Annual Product Reviews, Change Controls, Regulatory Submissions, Deviations, Validations, Procedures, PFDs, PFMEAs, etc.
- Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability.
- Identify opportunities and lead technical projects to improve process control and/or productivity.
- Serve as interface with upstream suppliers and parenteral product networks.
- Drive stability strategy for Concord products.
- Provide Audit support as needed.
- Identify opportunities and participate in projects to improve process control and/or productivity.
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
Entry Level
