QMS Job Description OSD / Injectable Pharma (5 Years Experience)
Implement and maintain QMS as per EU GMP, WHO-GMP, and applicable regulatory requirements.
Prepare, review, and control SOPs, protocols, formats, and quality records.
Handle deviations, CAPA, change control, and investigations.
Coordinate internal, external, customer, and regulatory audits.
Manage document control, training records, and data integrity compliance.
Review and track non-conformities, OOS/OOT investigations, and corrective actions.
Support batch record review and product quality investigations.
Coordinate with QA, QC, Production, Engineering, and Regulatory Affairs.
Prepare Quality Management Review reports and monitor quality KPIs.
Ensure compliance with cGMP requirements for OSD (Oral Solid Dosage) and injectable manufacturing.
Qualification: B.Pharm / M.Pharm / M.Sc. or relevant qualification. Experience: 2- 5 years in pharmaceutical QA/QMS, preferably in OSD and sterile injectable manufacturing.