Educational Qualification: B.Tech/M.Tech Biotechnology, B.Sc/M.Sc Biotechnology, B.Sc/M.Sc Microbiology. Job Description: Perform HPLC analysis of pharmaceutical/chemical samples (raw materials, intermediates, APIs, finished products). Prepare and standardise reagents, solutions, and reference standards. Document all analyses, results, and deviations as per Good Documentation Practices (GDP). Ensure proper calibration, maintenance, and troubleshooting of HPLC and other laboratory instruments (e.g., UV, IR, Dissolution apparatus). Review analytical data and ensure results are within specification. Follow Good Laboratory Practices (GLP), cGMP, and safety guidelines strictly. Participate in method validation, method transfer, and analytical investigations. Maintain laboratory records in accordance with regulatory requirements (e.g., FDA, EMA). Assist in audits and inspections by regulatory bodies and clients. Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹200,000.00 per year Benefits: Food provided Provident Fund Schedule: Rotational shift Work Location: In person

Educational Qualification: B.Tech/M.Tech Biotechnology, B.Sc/M.Sc Biotechnology, B.Sc/M.Sc Biochemistry. Perform line clearance activities before the start of manufacturing and packaging operations. Monitor critical in-process parameters during manufacturing and packaging (e.g., blending, compression, granulation, coating, filling, sealing). Perform in-process checks, including weight variation, hardness, thickness, disintegration time, leak tests, and reconciliation. Ensure compliance with batch manufacturing records (BMR) and batch packaging records (BPR). Review and verify process and cleaning validation activities on the shop floor. Handle deviations, change controls, incidents, and ensure timely documentation. Perform periodic GMP audits and maintain good documentation practices. Ensure sampling of in-process and finished products for quality control. Participate in investigations of non-conformities and CAPA implementation. Support regulatory and internal audits by providing documentation and on-floor guidance. Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹200,000.00 per year Benefits: Food provided Provident Fund Schedule: Rotational shift Work Location: In person

Educational Qualification: B.Tech/M.Tech Biotechnology, B.Sc/M.Sc Biotechnology, B.Sc/M.Sc Biochemistry. Perform line clearance activities before the start of manufacturing and packaging operations. Monitor critical in-process parameters during manufacturing and packaging (e.g., blending, compression, granulation, coating, filling, sealing). Perform in-process checks, including weight variation, hardness, thickness, disintegration time, leak tests, and reconciliation. Ensure compliance with batch manufacturing records (BMR) and batch packaging records (BPR). Review and verify process and cleaning validation activities on the shop floor. Handle deviations, change controls, incidents, and ensure timely documentation. Perform periodic GMP audits and maintain good documentation practices. Ensure sampling of in-process and finished products for quality control. Participate in investigations of non-conformities and CAPA implementation. Support regulatory and internal audits by providing documentation and on-floor guidance. Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹200,000.00 per year Benefits: Food provided Provident Fund Schedule: Rotational shift Work Location: In person

Educational Qualification: B.Tech/M.Tech Biotechnology, B.Sc/M.Sc Biotechnology, B.Sc/M.Sc Microbiology. Job Description: Perform HPLC analysis of pharmaceutical/chemical samples (raw materials, intermediates, APIs, finished products). Prepare and standardise reagents, solutions, and reference standards. Document all analyses, results, and deviations as per Good Documentation Practices (GDP). Ensure proper calibration, maintenance, and troubleshooting of HPLC and other laboratory instruments (e.g., UV, IR, Dissolution apparatus). Review analytical data and ensure results are within specification. Follow Good Laboratory Practices (GLP), cGMP, and safety guidelines strictly. Participate in method validation, method transfer, and analytical investigations. Maintain laboratory records in accordance with regulatory requirements (e.g., FDA, EMA). Assist in audits and inspections by regulatory bodies and clients. Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹200,000.00 per year Benefits: Food provided Provident Fund Schedule: Rotational shift Work Location: In person