Job Description

Coordinate with QA, QC, Purchase and Warehouse departments to ensure smooth production workflow.

Monitor raw material usage, production yield efficiency, and finished product quality.

Maintain cGMP compliance across all production processes and documentation systems.

Ensure proper shift-wise coordination and alignment of production targets.

Allocate equipment and utilities while ensuring adherence to production planning and safety standards.

Maintain updated documentation as per ISO, regulatory, and audit compliance requirements.

Key Responsibilities

• Coordinate daily production activities and documentation between departments.
• Monitor production performance including yield, material consumption, and process efficiency.
• Ensure strict compliance with cGMP standards in production operations.
• Maintain production records, batch documentation, and compliance reports.
• Support internal and external audits through proper documentation readiness.
• Work closely with QA, QC, warehouse and production teams to ensure process continuity.

Required Skills

• Strong knowledge of cGMP guidelines and production documentation practices.
• Experience in pharmaceutical, API, intermediate pharma, or chemical manufacturing industries.
• Good cross-department communication and coordination abilities.
• Analytical mindset for process efficiency and yield improvement.
• Understanding of production equipment operations and safety protocols.