Deputy Manager, Manufacturing Injectables

The role is responsible for ensuring current Good Manufacturing Practices (cGMP – Current Good Manufacturing Practices) compliance and supervising overall production activities in the injectable manufacturing area during the assigned shift. The incumbent ensures safe, compliant, and efficient sterile manufacturing operations, covering General, Control, and Aseptic areas. The role focuses on line readiness, validated and calibrated equipment status, documentation accuracy, and adherence to approved Standard Operating Procedures (SOPs – Standard Operating Procedures). It also involves reviewing and maintaining online production documents, coordinating with Quality Assurance (QA – Quality Assurance), Engineering, and Supply Chain teams, and driving consistent execution of production plans while complying with regulatory expectations, data integrity standards, and safety guidelines to ensure uninterrupted supply of high-quality injectable products.

• Ensure compliance with cGMP (Current Good Manufacturing Practices) and GDP (Good Documentation Practices) across General, Control, and Aseptic areas

• Supervise overall injectable production activities during the assigned shift

• Ensure all equipment and manufacturing lines are validated and calibrated before use

• Perform and verify line clearance activities prior to batch commencement

• Handle Change Control, Deviations, Investigations, and CAPA (Corrective and Preventive Action) processes

• Review, approve, revise, and implement SOPs (Standard Operating Procedures) for sterile manufacturing

• Monitor execution of production plan vs actual output on daily and monthly basis

• Ensure strict adherence to aseptic techniques and contamination control practices

• Oversee cleaning, sanitization, and environmental monitoring activities

• Coordinate with QA, QC, Engineering, and Warehouse for seamless operations

• Review and maintain online production and batch documentation

• Responsible for preparation & review of the all-master documents of production

• Responsible to update on self-hygiene

• Responsible to attend the training as per training schedule and to ensure training of the team as per TNI

• Support audit readiness and regulatory inspections as required

• Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.

• Responsible to give training to all the subordinates, technicians, and operators of the department. Responsible to update on self-hygiene.

• Responsible to attend the training as per training schedule and to ensure training as per TNI.

Qualifications

• B. Pharm B. Pharm - Required

• M. Pharm M. Pharm - Preferred

• 12 years or more in 12 - 15 Years