Glenmark Pharmaceuticals Opening: Quality Control Senior Officer

Glenmark Pharmaceuticals Recruitment Notification
  • Full Time
  • Aurangabad
  • 30000 INR / Month

Glenmark Pharmaceuticals Careers: Exciting Opportunity for Quality Control Senior Officer

Welcome to Glenmark Pharmaceuticals, a global pharmaceutical company committed to enriching lives through the development and manufacturing of high-quality medicines. As part of our expansion, we are delighted to announce the opening for the position of Quality Control Senior Officer at our Aurangabad Plant in Maharashtra, India.

About Glenmark Pharmaceuticals: Glenmark Pharmaceuticals is a leading player in the pharmaceutical industry, known for its commitment to innovation, quality, and excellence. With a global presence, we are dedicated to making a positive impact on healthcare by providing accessible and affordable medicines.

Company Vacancies List: Join our dynamic team with the following vacancy:

  • Position Title: Quality Control Senior Officer
  • Department: Quality Control
  • Location: Aurangabad Plant, Aurangabad, Maharashtra, India
  • Experience Range: 2 years – 8 years
Glenmark Pharmaceuticals Recruitment Notification
Glenmark Pharmaceuticals Recruitment Notification

Job Description: As a Quality Control Senior Officer, you will be responsible for:

  1. Adhering to cGMP and GLP standards in the Quality Control Department.
  2. Analyzing Raw Materials (RM), Packaging Materials (PM), Semi-Finished Goods (SFG), Finished Goods (FG), Stability, AMV, and Water, and calibrating analytical instruments.
  3. Coordinating with QA, store, and production for QC-related documentation requirements.
  4. Initiating work orders and ensuring timely completion of instrument qualification and maintenance.
  5. Sending samples to contract laboratories for analysis.
  6. Verifying SAP entries for accuracy.
  7. Managing primary, reference, and working standards and records.
  8. Operating, calibrating, and maintaining stability chambers and the stability management system.
  9. Performing stability-related activities in the SAP system.
  10. Managing HPLC columns within SOP timelines.
  11. Conducting GMP activities, including initiation of QMS in SAP and investigating LEIR, OOS, OOT, and Incidents.
  12. Preparing various documents as required in MS Office.
  13. Operating instrument software in the quality control department.

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