Executive
IndiaFull-time2–5 yrsPosted yesterday
Mid-level pharma role at RPG Group (CEAT, KEC, RPG companies). Needs 2+ years and a B.Sc, M.Sc or B.Pharm.
About the role
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.
What you'll do
- 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
What you need
- GMP
- SOP writing
- Documentation
- Communication
- Internal audit