Production Sterile - QMS - Trainee
Production Sterile - QMS - Trainee
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Job Description
QMS Support: Assist in the compilation and review of deviations change controls CAPA incident reports and related QMS documentation.
Training Documentation: Coordinate and maintain training matrices induction schedules attendance records and departmental SOP training logs.
Audit Preparation: Help prepare QMS documents and training records for regulatory and internal audits (e.g. USFDA MHRA WHO).
Compliance Tracking: Monitor compliance timelines for QMS activities and escalate delays to responsible stakeholders.
Document Control: Assist in SOP issuance retrieval version control and archival of controlled documents.
Learning & Development: Participate in structured on-the-job training related to GMP documentation QMS software/systems and compliance tools.
Required Experience:
IC
Employment Type
Contract
