About this role
- Follow cGMP, GDP, SOPs, and data integrity requirements.
- Ensure compliance with regulatory standards such as USFDA, MHRA, WHO-GMP, and EU-GMP where applicable.
- Participate in audits and support inspection activities ecord all production activities in BMR/BPR accurately and timely.
- Maintain equipment logbooks and cleaning records.
- Report deviations, breakdowns, and abnormalities immediately to the supervisor.
- Operate tablet compression machines as per approved Batch Manufacturing Records (BMR).
- Set up tooling, punches, dies, feeders, and machine parameters.
- Perform startup, in-process, and shutdown activities of compression equipment.
- Ensure proper machine cleaning and line clearance before batch commencement.