QC-Product/GLP/Inprocess/Central Lab (Sterile) Onesource Specialty Pharma Limited

2.0 - 7.0 years

3 - 8 Lacs

Hyderabad, Chennai, Bengaluru

Work from Office

Conduct routine and in-process testing of sterile products according to SOPs and GLP. Support Central Lab operations including sample preparation, testing, and documentation. Perform microbiological and physicochemical tests under sterile conditions. Record and report test data accurately in compliance with GLP and GMP standards. Maintain lab equipment, clean work areas, and follow aseptic techniques. Assist in investigations related to product quality deviations as needed. Follow safety, hygiene, and contamination control procedures strictly.

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QC-Investigations/Central Lab-Sterile Onesource Specialty Pharma Limited

10.0 - 20.0 years

10 - 20 Lacs

Hyderabad, Chennai, Bengaluru

Work from Office

Perform routine and non-routine QC testing in the Central Laboratory according to SOPs and regulatory requirements. Lead or support investigations related to out-of-specification (OOS), out-of-trend (OOT), and other quality deviations. Collect and analyze data to identify root causes and recommend corrective and preventive actions (CAPA). Collaborate with cross-functional teams (Quality Assurance, Production, R&D) during investigations and product release. Prepare and maintain accurate investigation reports, lab records, and documentation in compliance with GMP and corporate policies. Support stability studies, method validations, and lab audits. Ensure lab equipment calibration, maintenance, and compliance with safety standards.

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