Quality Control Jobs at Lupin | Apply Now for the Role
Are you looking for a rewarding opportunity in pharmaceutical quality control? Quality control jobs at Lupin offer an excellent chance to work with a global leader committed to high-quality, affordable healthcare. If you’re aiming to grow your career in QC and contribute to life-saving medicines, this position provides the perfect platform.
About Lupin: Lupin is a global pharmaceutical company offering a wide range of quality, affordable generic and branded formulations. Our company values innovation and the highest standards of quality in production and research to ensure that we meet our commitment to delivering life-saving medications to patients around the world.
Job Posting Date: 5 Dec 2025
Location: Mandideep – Bhopal, MP, IN
Company: Lupin
Job Description:
- Comply with all cGMP, GxP, or any other regulatory requirements, including EH&S requirements.
- Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
- Conduct all tasks/activities as per applicable SOPs, report any difficulty or deviation in following the procedures/instructions to immediate Supervisors/Managers.
- Report any quality concerns or suggestions for improvements to supervisors/Managers.
- Sampling, analysis, reporting and deposition of raw material injectable Raw material as per standard test procedure. Disposition of analysed samples after analysis and final approval.
- To ensure the OOS & OOT result is communicated to the concerned person.
- Sampling kit maintenance.
- To perform routine calibration of instruments/equipment.
- Review of documents related to quality control against the standard procedure, e.g., analytical raw data and calibration data, etc.
- To record and ensure the SAP entries of Raw material.
- Disposition of leftover samples.
- Maintaining the sampling booths in the warehouse.
- To initiate and investigate the laboratory incidents.
- Any other assignment allocated by the section in charge/department head.
- Filling of analytical records and submission to Doc-cell (as per applicability)
- Planning and coordination of Raw Material, executing and supervising all tasks and activities per the applicable SOPs.
- Authorised to print e-TDS from SAP for all types of QC samples. Reporting of events and abnormalities with preliminary investigation findings to the Reporting manager, HODs, functional heads, event investigation team, EHS department’s managers, and location head.
Work Experience: 2 to 5 yrs.
Education: Master’s in Chemistry
