Key Responsibilities
Coordinate with CMO/third-party manufacturing sites for QA activities.
Review BMR/BPR, COA, specifications, and other quality documents.
Coordinate deviations, OOS/OOT, CAPA, change controls, and investigations.
Monitor GMP compliance and quality standards at CMO sites.
Coordinate CMO audits and follow up on audit observations.
Support product release and ensure timely completion of quality documentation.
Maintain CMO QA records, trackers, and MIS.
Coordinate with QC, Regulatory, Supply Chain, and other departments.
Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
Experience: 2–5 years in Pharmaceutical QA; CMO/Third-Party experience preferred
Key Skills: GMP, GDP, QA Documentation, Deviation, CAPA, OOS/OOT, Change Control, Audit Coordination, MS Office and good communication skills.
Interested candidate can come for Interview on Below mentioned date & time
Interview Details:
Date: 4th September 2026 - 11th September 2026
Time: 11:00 AM to 2pm
Venue:
Kilitch Drugs India Ltd
37, Ujagar Industrial Estate
W.T. Patil Marg
Near Dukes Company
Deonar, Mumbai – 400088
Landmark: Next to D-Mart, Deonar
Nearest Railway Station: Govandi
Person to meet: Kalyani Thakur (HR)
Benefits:
Work Location: In person
