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You will be updated with latest job alerts via email Sterile Manufacturing Operations: Oversee aseptic filling compounding filtration and lyophilization processes to ensure product sterility and quality.
Aseptic Practices & Compliance: Ensure adherence to GMP USFDA MHRA WHO and EUGMP guidelines maintaining sterility assurance in cleanroom environments.
Process Monitoring & Validation: Perform inprocess 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 & Process Improvement: Identify and resolve manufacturing deviations aseptic failures and process inefficiencies to ensure continuous improvement.
Coordination & Training: Work closely with QA QC and Engineering teams and train staff on sterile handling gowning and aseptic techniques.
Required Experience:
Unclear Seniority
Full-Time