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 will be preferred...