Production - QMS
Responsibilities
- Monitor and supervise daily production operations to meet planned targets.
- Coordinate with maintenance, QA, and warehouse teams for smooth operations.
- Ensure line clearance before starting production activities.
- Troubleshoot process issues and minimize downtime.
- Prepare, review, and maintain Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
- Ensure all entries are accurate, complete, and in compliance with GMP guidelines.
- Record deviations, incidents, and corrective actions in documentation.
- Ensure real-time documentation during manufacturing and packaging activities.
- Maintain proper archival and retrieval of records.
Qualifications & Experience
- Bachelor's degree in pharmacy / chemistry.
- 1–5 years of experience in production (preferably pharma or regulated industry).
- Good knowledge of GMP and documentation practices (BMR/BPR).
