Job Description
Ensure pharmaceutical manufacturing activities comply with GMP, regulatory and quality standards while supporting efficient production, maintaining accurate documentation, and assisting with shift operations.
Main Responsibilities
- Support production activities to meet schedules
- Verify products, equipment, materials, and production areas for GMP compliance
- Review and approve production documentation, line clearances, and batch records
- Ensure manufacturing processes comply with quality, GMP, and regulatory standards.
- Investigate production issues and implement corrective actions
- Initiate, investigate, document and close deviations.
- Coordinate and assess change controls and its actions to ensure compliance and minimize compliance risk.
- Develop and track Corrective and Preventive Actions (CAPAs) to address root causes and prevent recurrence
- Drive process improvement initiatives to ...
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