Role & responsibilities
To ensure effective compliance of quality management system as per cGMP and international regulatory requirement in production and ancillary areas.
Responsible for implementation of systems, processes and procedures to facilitate smooth functioning of overall operations.
To ensure the execution and maintenance of validated status of the injection facility.
To ensure effectiveness of all standard operating procedures, batch document, master documents of production and compliance to documents.
Assuring that the department is in compliance with cGMP/regulatory requirements.
Co-ordination for recent product transfers and thereafter support for process validations.
Co-ordination with QA for self-inspection and compliance to the audit observations.
Responsible for improvement in product yield and productivity.
Proper utilization of man and machine and to ensure compliance for documents as per cGMP requirements.
To prepare and review capex, user requirement specification etc.
To prepare and review MIS report and other related documents of production department as per requirements.
To ensure that initial and continuing training of production persons has been performed as per schedule.
To confirm the training matrix,



training reports of new and existing employees.
To ensure scheduled validation of the equipment, calibration of devices and maintenance of equipments.
Responsible for planning and implementation of preventative and predictive maintenance schedules.
Overseeing the recruitment, performance of subordinates, mentoring/inspiring them to improve their contribution levels.
Responsible for man management and administrative functions and recent Project management.
Responsible for implementation of system, processes and procedures to facilitate smooth functioning of overall operations enhance operational efficiency and cost optimization.
Market compliant investigation jointly with QA and other CFT’s.
To comply and ensure the implementation of safety practices.
To report that entire daily schedules and executions to the management.
Responsible for self-Inspection as per schedule.
Review and approval of QMS elements and process documents through ample logic and EDCS system.
Review and approval of RM, PM, consumable and other dispensing activities through ERP system.

Preferred candidate profile

📌 Manager Production Sterile Facility Himachal Pradesh
🏢 Immacule Life Sciences
📍 Himachal Pradesh