Job Description
Responsibilities:
- Responsible for primary contact of quality on the floor, particularly in the Visual Inspection Training, Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards.
- Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations
- Maintain regulatory compliance in accordance with cGMP practices
- Ensure manufacturing policies and procedures conform to Pfizer standards
- Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Associate or Sr. Team Leader
- Review of Batch reports and Equipment audit trails
- Perform Acceptable Quality level sampling, Inspection in VIDT and Batch record review and release
- Perform batch start-up and end activities viz. sensor challenge tests, recipe review, etc
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