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.... 
    Suggested
    Full time

    USV

    Diu
    a month ago
  •  ...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... 
    Suggested
    Full time

    USV

    Diu
    a month ago
  •  ...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... 
    Suggested
    Full time

    USV

    Diu
    a month ago
  •  ...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... 
    Suggested
    Full time

    USV

    Diu
    a month ago