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.

📌 QA QMS officer (Baddi)
🏢 Hr Services Chandigarh
📍 Baddi