DGM production

You should have experience working in a Managerial capacity in Pharmaceutical API Intermediate/CDMO manufacturing set ups. Your responsibilities will include: - Managing daily production activities according to the monthly plan - Improving and monitoring yield and quality - Ensuring raw material planning in coordination with the Stores Department - Monitoring and reducing production cycle time - Preparing monthly reconciliation reports - Effectively managing available resources and manpower - Ensuring all processes are carried out in accordance with cGMP guidelines in coordination with the Quality Assurance Department - Reviewing filled Batch Production Records (BPR) after batch completion - Reviewing BPR, Standard Operating Procedures (SOP), validation protocols, and other production-related documents - Initiating change control for any changes in production activities - Evaluating, investigating, and reporting critical deviations, Out Of Specification (OOS) results, complaints, and material returns - Providing training to production employees and reviewing performance standards Qualifications required for this role include: - BE in Chemical Engineering (Note: No additional details about the company were mentioned in the job description),