Production Supervisor- Pharmaceutical Manufacturing

Role Overview: As a Production Supervisor in Pharmaceutical Manufacturing at Makshi, Madhya Pradesh, your role will involve supervising daily production operations to ensure compliance with Good Manufacturing Practices (GMP). You will be responsible for overseeing the production of tablets, capsules, liquids, or injectables, ensuring adherence to Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and Standard Operating Procedures (SOPs). Additionally, you will monitor equipment readiness, coordinate with Quality Assurance/Quality Control (QA/QC) for in-process checks, maintain shop floor hygiene and discipline, and train staff on GMP, Good Distribution Practices (GDP), and safety protocols. Your role will also involve ensuring timely documentation for audits, handling deviations, change controls, Corrective and Preventive Actions (CAPA), and managing inventory of raw materials and tools. Key Responsibilities: - Supervise production of tablets, capsules, liquids, or injectables - Ensure adherence to BMR/BPR and SOPs - Monitor equipment readiness and maintenance - Coordinate with QA/QC for in-process checks - Maintain hygiene and discipline on the shop floor - Train staff on GMP, GDP, and safety - Ensure timely documentation for audits - Handle deviations, change controls, and CAPA - Support validation and regulatory compliance - Manage inventory of raw materials and tools Qualifications & Skills: - B.Pharm / M.Pharm / B.Sc in Chemistry or Life Sciences - Valid Manufacturing Chemist License (Form 25/28) - Strong understanding of GMP, Schedule M, and documentation - Experience in team handling and shift operations - Familiarity with audits and data integrity - Communication skills in Hindi and English; leadership skills Preferred Attributes: - Exposure to solid dosage or sterile manufacturing - Process-driven and quality-conscious - Capable of managing timelines and cross-functional coordination Job Type: Full-time *Health insurance provided* (Note: No additional details of the company were mentioned in the provided job description),