Key Responsibilities:
Handle QMS activities including CAPA, Change Control, Deviation, and OOS/OOT.
Prepare, review, and maintain QMS documentation as per cGMP and regulatory guidelines.
Support internal audits, external audits, and regulatory inspections.
Ensure timely closure of quality incidents and continuous improvement initiatives.
Coordinate with cross-functional teams for compliance and quality culture.
Requirements:
B.Pharm / M.Sc (Chemistry) with 3–6 years of QMS experience in pharma formulation industry.
Sound knowledge of cGMP, documentation practices, and regulatory standards.
Robust communication and documentation skills.
Why Join Us?
Chance to work in a dynamic formulation setup with exposure to global quality standards and growth opportunities.