Role & responsibilities: Support QA operation and ensure GMP and regulatory compliance. Manage QMS, audits, CAPA and other QMS related documents in plant.
Ensure data integrity, documentation compliance and continuous improvement.
review and approve batch records, SOPs, validation documents and quality records.
Preferred candidate profile: B.Pharm, M.Pharm, or M.Sc. with hands-on experience in QA and QMS activities in a pharmaceutical manufacturing plant. Candidates should have experience handling regulatory audits and preparing audit compliance/CAPA responses.
*Candidates whose hometown is Bhavnagar or who are willing to relocate to Bhavnagar will be preferred.*