Executive export documentation jobs in Diu

 ...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.... 

 ...Position Overview The Executive Microbiologist is responsible for execution, review, and compliance of microbiological testing activities...  ...and disposal of microbial cultures as per biosafety norms. Documentation & GMP Compliance Prepare, review, and maintain... 

 ...Plan, execute, and monitor cleaning validation and verification activities for manufacturing equipment and facilities. Identify worst...  ...during new product introductions or equipment changes. Documentation & Protocol Management Draft, review, issue, and maintain cleaning... 

 ...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... 

 ...analytical instruments. Ensure compliance with USFDA, cGMP, ALCOA+, and data integrity requirements. Maintain instrument lifecycle documentation, logbooks, calibration records, and SOPs. Coordinate with external service engineers and instrument vendors. Support... 

 ...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... 

 ...meeting production targets. Key Responsibilities Supervise and execute production operations for granulation, compression, coating,...  ...departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and other regulatory guidelines... 

 ...Job Title Senior Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12A/G12B Location...  ...process qualification batches To prepare and review new product documents like material requirement sheet, master formula card, bill of... 

 ...Job Purpose To plan, execute, and deliver engineering projects in a USFDA‑approved OSD manufacturing facility, ensuring compliance...  ...mechanical engineering works. 4. Compliance, Validation & Documentation Ensure all projects comply with USFDA, cGMP, EHS, and internal... 

 ...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... 

 ...in the global plastic packaging industry. Role Description This is a full-time, on-site position for a Quality Control Executive located in Daman. Responsibilities include conducting quality and laboratory tests, ensuring calibration of equipment, and maintaining... 

Job Description : Regional Sales Manager About the role: Regional Sales Manager is core to growing business on TenderHealthtech consult platform. The person is responsible for the business growth and majorly driving product adoption for making the consult platform an ...