: Responsible for ensuring all documentation, including standard operating procedures (SOPs), batch manufacturing records (BMR), and batch packaging records (BPR), is accurate, complete, and compliant with regulations.
Compliance Monitoring
: Monitors all manufacturing and laboratory operations to ensure strict adherence to internal policies and external regulations such as GMP, HACCP, and relevant local health authority requirements (e.g., FSSAI, USFDA).
Audits and Inspections
: Conducts regular internal audits and prepares the facility for external audits and regulatory inspections, managing all related documentation and corrective actions.
In-Process Quality Assurance (IPQA)
: Performs on-the-floor checks during production, including line clearance verification, environmental monitoring, and in-process product testing (e.g., weight variation, hardness, disintegration).
Deviation and CAPA Management
: Investigates any deviations, discrepancies, or non-conformities during production using root cause analysis, and develops and tracks Corrective and Preventive Actions (CAPAs).
Material Release
: Reviews documentation and test results for raw materials, packaging materials, and finished products, and has the final authority to approve or reject them for use or release to the market.
Training
: Develops and delivers training programs to production and lab personnel on quality-related procedures, GMP, and safety protocols.
Continuous Improvement
: Utilizes quality metrics and data analysis to identify areas for improvement and leads initiatives to optimize processes and reduce waste.
Job Types: Full-time, Permanent
Pay: ₹240,894.83 - ₹322,389.80 per year
Work Location: In person
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