QC Officer

Job Description

Key Responsibilities: Conduct chemical, physical, and microbiological testing of raw materials, intermediates, and finished products. Perform sampling, analysis, and release of packaging and labeling materials. Operate and calibrate laboratory instruments (e.g., HPLC, GC, UV-Vis Spectrophotometer, pH meter). Prepare and maintain records of all tests in accordance with GMP and regulatory requirements. Maintain laboratory cleanliness, safety, and documentation standards. Review and verify analytical data and test results for accuracy. Investigate out-of-specification (OOS) and out-of-trend (OOT) results and assist in root cause analysis. Ensure timely reporting of test results to support production and release schedules. Participate in method development and validation activities when required. Follow and enforce Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Support internal and external audits and inspections. Qualifications: Bachelor’s degree in Pharmacy, Chemistry, Biochemistry, or a related field. 1–3 years of experience in a QC laboratory, preferably in the pharmaceutical industry. Familiarity with regulatory standards (e.g., USFDA, MHRA, WHO, EUGMP). Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per year Benefits: Provident Fund Schedule: Day shift Fixed shift Experience: QC: 2 years (Required) Work Location: In person