- Execute daily production activities as per the approved production plan and shift schedule.
- Supervise shift personnel and ensure optimum manpower utilization.
- Ensure API manufacturing operations are performed as per approved SOPs, BMRs, and GMP requirements.
- Monitor batch processing, equipment operation, process parameters, and production yield.
- Ensure timely completion of batch manufacturing records and other production documentation.
- Maintain compliance with GMP, GDP, EHS, and data integrity requirements.
- Coordinate with QA, QC, Engineering, and Warehouse teams for smooth production operations.
- Ensure proper line clearance, equipment cleaning, and area readiness before starting operations.
- Monitor deviations, process abnormalities, and equipment breakdowns; report and escalate issues promptly.
- Ensure adherence to safety procedures, PPE requirements, and chemical handling practices.
- Maintain housekeeping, 5S, and cleanliness standards in the production area.




- Prepare shift handover reports covering batch status, equipment condition, manpower, and pending activities.
- Support investigations, CAPA implementation, and continuous improvement initiatives.
- Ensure achievement of production targets while maintaining quality, safety, and regulatory compliance.Role & responsibilities

Preferred candidate profile

- Qualification & Experience: B.Sc./M.Sc. Chemistry, B.Pharm, or Chemical Engineering with 36 years of experience in API manufacturing.
- Technical Knowledge: Valuable understanding of cGMP, SOPs, BMRs, batch processing, API manufacturing equipment, and pharmaceutical documentation.
- Key Competencies: Strong shift management, manpower handling, problem-solving, safety awareness, and coordination with QA/QC and other departments.

📌 Shift Incharge - API Production (Patiala)
🏢 Valence Labs
📍 Patiala