Key Responsibilities

• Perform in-process quality checks during manufacturing and packing of injectable products.
• Conduct line clearance activities before and after production operations.
• Monitor critical process parameters and ensure compliance with approved procedures.
• Verify batch manufacturing records (BMR) and batch packing records (BPR).
• Ensure adherence to SOPs, cGMP, GDP, and regulatory guidelines.
• Monitor aseptic practices and cleanliness in sterile manufacturing areas.
• Perform sampling and in-process testing as per specifications.
• Coordinate with Production, QA, and Microbiology departments for smooth operations.
• Identify and report deviations, incidents, and non-conformities.
• Support investigations, CAPA implementation, and audit readiness activities.
• Maintain accurate documentation and IPQC records.
• Ensure calibration status and proper usage of instruments/equipment.