Job Description – Injectable Manufacturing (Aseptic Operations)Operate and monitor aseptic equipment (vial/syringe filling lines, isolators, depyrogenation tunnel, autoclaves, lyophilizers, formulation vessels, sealing machines). Ensure c GMP-compliant production operations with accurate real-time documentation. Prepare and review SOPs, BMRs, and perform SAP entries. Support equipment qualification/validation and routine production activities. Ensure area and equipment cleaning as per approved SOPs. Monitor BMS parameters (temperature, differential pressure, humidity) and maintain records. Handle QMS elements: deviations, change controls, and CAPA. Prepare risk assessments, protocols, study reports, and technical documents. Review production records for compliance and completeness. Train personnel on c GMP, SOPs, BMRs, and Valuable Documentation Practices (GDP). Experience - 0-6 Months Preferred - Male Candidates Qualification - B. Pharm Timings - Must be available for rotational shift.