- 2–5 years
Responsibilities
- Maintain and control SOPs, protocols, reports, formats and other QA documents.
- Ensure preparation, review, approval, issuance and distribution of controlled documents.
- Maintain document issuance, revision history and archival records.
- Ensure timely review and revision of SOPs and other controlled documents.
- Maintain proper documentation practices as per cGMP and ALCOA+ guidelines.
Requirements
- B.Pharm
- M.Pharm
- B.Sc
- M.Sc
- Nice to have: Experience in OSD (Oral Solid Dosage) manufacturing