Key Responsibilities

- QMS Compliance & Documentation
- Prepare, review, and maintain SOPs, Batch Manufacturing Records (BMR), and related production documents.
- Ensure timely closure of deviations, change controls, and CAPAs related to production activities.
- Maintain compliance with global regulatory standards.
- Batch Execution & Monitoring
- Monitor batch manufacturing processes to ensure adherence to approved procedures.
- Coordinate with QA for line clearance and in-process checks.
- Deviation & Investigation Handling
- Initiate and investigate production-related deviations.
- Prepare investigation reports and implement corrective and preventive actions (CAPA).
- Training & Compliance
- Conduct training for production staff on cGMP, SOPs, and QMS requirements.
- Ensure readiness for regulatory audits and inspections.

- Continuous Improvement
- Participate in root cause analysis and process improvement initiatives.
- Support implementation of data integrity practices and electronic documentation systems.

📌 Qms Executive (Neemrana)
🏢 Stanford Laboratories
📍 Neemrana