Associate - QA Master Data Steward
Lilly•Lebanon, IN
•Onsite
About The Position
This role acts as a data steward in SAP and LIMS for specifications. This role will develop these programs for the new LP1 facility in accordance with GQS guidelines and the IT systems in use at the LP1 plant.
Requirements
- BS in Engineering or science related field
- 3+ years in pharmaceutical industry
- 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 and 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
- Previous experience in pharmaceutical industry
- Previous experience in QA, TS/MS QC or Engineering
- Prior work with cGMPs or external regulations
- Previous experience with root cause investigations
Responsibilities
- Develop and provide oversight to the Specification program
- Manage master data in SAP and LIMS at startup and routine manufacturing
- Support data management for change controls and deviations
- Prepare for and participate in internal and external regulatory inspections
- Acts as a liaison for US and OUS customers toward resolution of concerns from customers.
Benefits
- company bonus
- 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
