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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 cGMP-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 cGMP, SOPs, BMRs, and Good Documentation Practices (GDP).
Experience - 0-6 Mont
hs Preferred - Male Candidat
es Qualification
- B. Pha
rm Timings - Must be available for rotational shif
t.
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