Quality Control Jobs at Lupin | Chemistry Graduates Apply Now
Are you looking for Quality Control Jobs in the pharmaceutical industry with a reputed organization? Lupin is hiring an Officer – Quality Control at its Mandideep (Bhopal) facility. This role under Lupin Jobs offers hands-on exposure to cGMP, SOP compliance, raw material analysis, and laboratory investigations, making it a strong opportunity for professionals seeking long-term growth through Lupin Careers.
- Location Mandideep – Bhopal, MP, IN
- Company Lupin
About Lupin
Lupin is a globally recognized pharmaceutical company known for its strong commitment to quality, innovation, and regulatory compliance. With a significant presence in India and international markets, Lupin offers excellent growth opportunities through Lupin Careers. Professionals joining through Lupin Jobs gain exposure to world-class manufacturing, quality systems, and continuous learning, making Lupin a preferred employer for Quality Control Jobs in the pharmaceutical industry.
Job Description
- Compliance: Comply with all cGMP, GxP, or any other regulatory requirements, including EH&S requirements.
- Training: Complete training on relevant SOPs and develop an understanding of the activities to be conducted before undertaking any task.
- Task Execution: Conduct all tasks/ activities as per applicable SOPs, report any difficulty or deviation in following the procedures/instructions to immediate Supervisors/Managers.
- Quality Concerns: Report any quality concerns or suggestions for improvement to supervisors/Managers.
- Raw Material Management: Sampling, analysis, reporting, and deposition of raw material injectable. Raw material as per the standard test procedure. Disposition of analyzed samples after analysis and final approval.
- Communication: To ensure the OOS & OOT results are communicated to the concerned person.
- Maintenance: Sampling kit maintenance.
- Calibration: To perform routine calibration of instruments/ equipment.
- Document Review: Review of documents related to quality control against the standard procedure, e.g., analytical raw data and calibration data, etc.
- SAP Entries: To record and ensure the SAP entries of Raw material.
- Sample Disposition: Disposition of leftover samples.
- Warehouse Maintenance: Maintaining the sampling booths in the warehouse.
- Incident Investigation: To initiate and investigate the laboratory incidents.
- Additional Assignments: Any other assignment allocated by the section in charge/department head.
- Analytical Records: Filling of analytical records and submission to Doc-cell (as per applicability).
- Planning and Coordination: Planning and coordination of Raw Material, executing and supervising all tasks and activities per the applicable SOPs.
- Authorization and Reporting: Authorize 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 the location head.
Work Experience
Experience: 2 to 5 yrs.
Education
Master’s in Chemistry
Graduation in Pharmacy
