Supervise and manage production activities in API, bulk drugs, or pharmaceutical manufacturing.Ensure production processes comply with cGMP standards and FDA regulations.Maintain accurate production records and documentation as per cGMP guidelines.Monitor workflow, coordinate with team members, and ensure timely completion of production targets.Troubleshoot production issues and implement corrective actions to maintain product quality.Ensure adherence to safety, quality, and operational protocols on all shifts.Skills Required
Shift Management, Production Planning, Quality Control