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Full-time
- Must have cGMP and minimum ICHQ7 pharmaceutical manufacturing experience.
- Coach and Lead operations crew with day-to-day tasks and cGMP practices.
- Draft and revise official manufacturing documents, SOPs, and Batch Records.
- Lead initiation and closure of deviations; may serve as the lead in the departmental investigation and be responsible for closing out deviations and CAPAs∯*∯ GMP batch review and close-out with Quality Assurance group.
- Collaborate with development groups to assist with tech-transfer, scale-up, and translation activities.
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