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This leader will be instrumental in ensuring robust manufacturing processes, seamless technology transfers, scale-up, validation, and lifecycle management of drug substance and drug product across our portfolio. This is a highly visible role at the
Assess, review and approve quality records and release files/dossiers e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions, complaints, APR/PQRs, in line with current local SOPs. Act as QA contact for specific projects
Ensuring the sterility of injectable products through robust contamination control and sterility assurance strategies. This role extends beyond microbiological testing to encompass comprehensive oversight of aseptic manufacturing