Job Description

Job summary
We are looking for a meticulous professional to lead drug product manufacturing and sterile formulation operations, ensuring adherence to Current Positive Manufacturing Practice (cGMP) and safety norms. Your focus on drug product validation within defined timelines and volumes, while maintaining compliance with quality standards and regulatory requirements, is crucial to the organization's commitment to excellence in pharmaceutical production.

Roles & Responsibilities
• You will be responsible for receiving inputs from production planning and preparing the monthly operation plan on the production floor, encompassing scheduling, staffing, monitoring, training, and troubleshooting to ensure that all operations comply with applicable BPRs/EBRs (Batch Production Record/Electronic Batch Record), SOP (Standard Operating Procedures), and safety guidelines.
• Your role involves understanding and administrating contract manpower, supporting capacity supply and planning, monitoring and controlling production schedules, and preparing the annual production budget.
• You will be responsible for reviewing and approving SOPs, protocols, reports, discrepancies, change requests, CAPA (Corrective and Preventive Actions), QRM (Quality Risk Management), and batch and packaging records.




• Your role will include collaborating with cross-functional departments to close discrepancies and implement corrective actions, ensuring compliance with relevant GMP (Good Manufacturing Practices), safety standards, and SOPs for designated manufacturing equipment.
• Your role includes completing batch documentation in compliance with GMP, collecting and maintaining data, and participating/leading in quality and safety investigations to address and improve CAPA for drug product manufacturing & sterile formulation operation.
• You will be responsible for maintaining manufacturing equipment for functionality and calibration compliance, operating manufacturing equipment and automated systems within validated process parameters, and actively promoting safety awareness and improvements.
• You will engage in continuous improvement activities, adhere to safety rules, and report any unsafe matters or near misses/accidents.
• You will be responsible for goal setting and performance reviews, training, and coaching employees, effectively managing employee performance issues and corrective actions, recognizing and appreciating employee contributions, and undertaking activities to support the achievement of individual, departmental, and business objectives.

📌 Team Lead - Drug Product (Hyderabad)
🏢 Dr. Reddy's Laboratories
📍 Hyderabad