Ajanta Pharma Limited, a leading name in the pharmaceutical industry, is inviting applications for the role of Officer – Quality Assurance at its US FDA-approved formulation facility located in Paithan, District Chhatrapati Sambhajinagar, Maharashtra.
Role Overview
This position offers a dynamic opportunity for qualified professionals to contribute to quality assurance operations in a regulated Oral Solid Dosage (OSD) environment. The selected candidate will play a key role in maintaining compliance, ensuring documentation integrity, and supporting analytical review processes.
Key Responsibilities
•OSD formulation experience in FDA-approved manufacturing setups
•Quality Management System (QMS) oversight and documentation review
•Analytical record evaluation and lab QA coordination
•Trending and reporting on QMS activities including change control, CAPA, investigations, deviations, and risk assessments
•Proficiency in Microsoft Office tools (Excel, Word, PowerPoint, Outlook)
Eligibility Criteria
•Educational Qualification: B.Pharm / M.Pharm / M.Sc.
•Candidates must demonstrate hands-on experience in pharmaceutical QA functions and regulatory compliance.
Application Details
Interested candidates are encouraged to share their updated resume at cv.ptn@ajantapharma.com. This opportunity remains open until November 12, 2025.
📍 Location: Ajanta Pharma Limited, B-4/5/6, MIDC Area, Paithan, Dist. Chhatrapati Sambhajinagar, 431148


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