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QA Representative - Floor Support
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Full-time
- Knowledge of cGMP practices including good documentation practices, data integrity and regulatory compliance
- Function as a cGMP liaison, working with Global Facility Delivery and Lilly project staff to complete the detailed design of the assigned areas employing QbD and QRM principals and ensuring the integration of Global Quality System requirements into the design
- 3+ years' experience in Quality pharmaceutical manufacturing required
- Demonstrated knowledge and use of US, EU, Japan and other regulations in the area of pharmaceutical manufacturing
- Ability to work 8-12 hour shifts onsite (not eligible for remote work)
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