Average salary: Rs745,000 /yearly
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- ...analytical methods as per regulatory guidelines (USFDA EU ICH). Execute calibration qualification (IQ/OQ/PQ) and periodic review of QC... ...and CAPA implementation related to validation. Maintain documentation and records in line with cGMP and data integrity requirements....SuggestedFull time
- ...in-process checks review batch records and support media fill validation sterility testing and equipment qualification . Documentation & Batch Records: Maintain BMR/BPR deviation reports and compliance documentation as per regulatory standards. Troubleshooting...SuggestedFull time
- ...Production Planning & Execution: Oversee the daily production schedule for GranulationCompressionand Coating to ensure timely delivery... ...principles. QMS Ownership: Lead the investigation and documentation of Deviations Change Controls and CAPAs .Ensure all Out of Specification...SuggestedFull time
- ...differentials in production areas. Preventive Maintenance (PM): Execute the PM schedule for all utility equipmentincluding motor control... ...using root cause analysis (RCA) and ensure that repairs are documented in compliance with cGMP standards. Statutory Compliance: Coordinate...SuggestedFull time
