Looking to take your pharmaceutical career to the next level? Glenmark Pharmaceuticals is hiring for the position of In-process Quality Assurance (IPQA) Officer at its Nashik facility. This is a golden opportunity for B.Pharm or M.Pharm professionals with 3–6 years of experience in external preparations, ointments, and oral solid dosage (OSD) IPQA activities. Join one of India’s leading pharma giants and play a critical role in ensuring top-notch quality standards across manufacturing and packaging processes.
About Glenmark Pharmaceuticals
Glenmark Pharmaceuticals is a leading global innovative pharmaceutical company committed to enriching lives through high-quality healthcare solutions. Headquartered in Mumbai, Glenmark is recognized for its R&D-driven approach, manufacturing excellence, and robust global presence. The company focuses on therapeutic areas such as dermatology, respiratory, and oncology, with a growing emphasis on biologics and specialty products.
Job Details:
Job Title: In-process Quality Assurance Officer
Location: Nashik, India
Function: Quality Assurance
Educational Qualification: B. Pharm / M. Pharm
Experience: 03 – 06 years of experience in external preparations, Ointment, and OSD IPQA activities
Job Location: Nashik
Job Responsibilities
- To track batches for process validation, packing validation, and hold time study.
- Certification of Appropriate and timely Line-Clearance for Manufacturing, Packing, Dispensing & coding.
- To carry out the online in-process checks & to take online SAP entries.
- To withdraw & Submit the Samples (Analysis SFG and FG & Control samples, Validation, Regulatory, R&D, Hold time study & Micro samples) to the Concern Dept. as & when required.
- To ensure cGMP on the shop floor and to highlight online Problems/nonconformance concerning Procedures, Specifications, SOPs, cGMP, etc., daily. The Number of critical/major nonconformances noticed.
- Online BPR, Logbook completion, and review of documents like Preventive maintenance, calibration records, daily/weekly cleaning, quarantine register, etc., in the Concerned department.
- Issuance of Batch Manufacturing Records and Batch Packing Records to the production department.
- Review of Executed Batch Manufacturing Records and Batch Packing Records.
- To verify online finished goods before transfer to BSR.
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