Full-time Posted June 04, 2026
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Job Description

Job Responsibilities

  • Handling and troubleshooting of sterile manufacturing and filling equipment.
  • Managing equipment breakdown activities, root cause analysis, and CAPA implementation.
  • Preparation, review, and execution of equipment qualification documents and technical documentation.
  • Monitoring preventive maintenance activities to ensure minimum equipment downtime.
  • Execution and monitoring of production and engineering activities in compliance with cGMP requirements.
  • Preparation and review of SOPs, protocols, reports, and other GMP documentation.
  • Ensuring adherence to aseptic practices and cleanroom behavior standards.
  • Independently handling and managing shopfloor activities effectively.


Eligibility Criteria

  • Minimum 6 years of relevant experience in sterile pharmaceutical manufacturing facilities.
  • Candidates from sterile injectable pharmaceutical facilities wi...

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