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- ...initiatives. Regularly collect analyze and report data to ensure evidence-based decision-making and continuous program improvement. Documentation of ground stories in the form of Case studies and Success stories. Candidate Profile: We are looking for individuals who...SuggestedLocal areaWorldwide
- ...Lubrication & Upkeep: Execute systematic greasing and oiling of machine parts using pharma-grade lubricants to ensure smooth operation. Documentation Learning: Maintain equipment logbooks and assist in updating equipment history cards and PM checklists. Workshop Activities:...SuggestedContract workTraineeshipInternship
- ...Breakdown Analysis: Lead the troubleshooting of electrical failures using root cause analysis (RCA) and ensure that repairs are documented in compliance with cGMP standards. Statutory Compliance: Coordinate with external agencies for mandatory inspectionssuch as CEIG...SuggestedFull time
- ...Conduct regular checks of equipment performance lubrication and utilities such as HVAC compressed air and water systems. Documentation: Fill out maintenance logs breakdown reports and equipment history records as per GMP and SOP requirements. Cleanroom Compliance...SuggestedFull time
- ...report preparation and implement recommended actions. 5. Deliver SOP training to train a team on specific processes changes in the documents and CAPA. 6. Handling of miscellaneous documents (Protocols & Report). 7. Tracking and Implement changes to the documents as per...SuggestedFull time
- ...Trial Monitoring: Supervise Scale-up and Exhibit batches to identify critical process parameters (CPPs) and ensure consistency. Documentation: Draft and review Technology Transfer Dossiers (TTD) Process Validation Protocols and Master Formula Records (MFR)....SuggestedFull time
- ...Manage the collection of in-process samples blend samples stability samples and reserve samples according to the sampling plan. Documentation Review: Real-time review of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) to ensure data integrity and...SuggestedFull time
- ...vendors for purchase of critical machines/spares. 4. Follow up for receipt of imported machines/spares. 5. Review change control document (post-installation). 6. Provide inputs for preparation/updation of engineering drawings. 7. Develop the preventive maintenance procedure...SuggestedFull time
- ...Support the Training Coordinator / Department Training Coordinators (DTCs) in scheduling and tracking training sessions. Learn documentation control data integrity practices and archiving requirements. Ensure confidentiality and accuracy while handling plant...SuggestedContract workInternship
- ...Sanitation: Execute Type A (Minor) and Type B (Major) cleaning of machines tools and processing areas as per validated SOPs. Documentation Learning: Learn to record real-time data in Batch Manufacturing Records (BMR) machine logbooks and weighing slips under supervision...SuggestedContract workTraineeshipInternship
- ...) and Batch Packing Records (BPR) to ensure 100% compliance with ALCOA principles. QMS Ownership: Lead the investigation and documentation of Deviations Change Controls and CAPAs .Ensure all Out of Specification (OOS) incidents in production are addressed and closed....SuggestedFull time
- ...Loading: Coordinate the transfer of washed vials into the Tunnel Sterilizer (Depyrogenation Tunnel) for drying and sterilization. Documentation: Accurately fill out Equipment Logbooks and Batch Manufacturing Records (BMR) noting start/end times and utility parameters....SuggestedFull time
- ...-Grade lubricants for all moving parts and maintain a critical spares inventory to reduce Mean Time to Repair (MTTR). Logbook Documentation: Accurately record all maintenance activities parts replaced and machine Down Time in the equipment history cards and maintenance...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
- ...machines (Linear or Rotary) ensuring correct mechanical settings for various vial sizes (2ml to 100ml). Utility Management: Monitor and document the pressure and temperature of WFI (Water for Injection) Purified Water and Compressed Air used in the cleaning cycles....SuggestedFull time
- ...activities. Participate in investigations deviations OOS/OOT results and CAPA implementation related to validation. Maintain documentation and records in line with cGMP and data integrity requirements. Coordinate with cross-functional teams during audits and...Full time
