Job Description

Education : B. Pharm

Experience : 14.2 Years

Job responsibles * Authorized to sign as a doer & also authorized to sign as a checker/verifier in

• Master Batch manufacturing record, Area cleaning & sanitization logbook/formats, etc.
• Risk assessment, process validation protocol, Incident and Investigation report,

• CAPA plans and closure, Protocols & reports, URS,
• Internal Quality Audit Compliance and closure.
• Change control, Standard Operating Procedure (SOP)
• Any other documents used for the execution of activities.
• Overall responsible for the production activity related to production department.
• Responsible for establishing new procedures, maintaining and updating existing procedures in the production department.
• Responsible to co-maintain, along with the Quality Assurance manager, GMP in production department.
• Responsible for establishing a system in accordance with Good Manufacturing Practice guidelines.
• Responsible for Good Manufacturing Practice training to staff in the Sterile and non-sterile departments.
• To co-ordinate with FDD for Exhibit batches of new Products.
• To co-ordinate with Quality control department in matters relating to product quality.
• Responsible for production planning schedule, control and execution.
• Responsible for optimization of the resources namely men, material and machine in budgetary norms.
• To make daily/monthly reports to the management on achieving the activity concerning the management.
• To co-ordinate with the Engineering department for preventive maintenance schedule.
• To co-ordinate with Warehouse for the materials to achieve schedule plan.
• To undergo functional training, cGMP training or any other training identified as per schedule.
• Any other responsibility assigned by department head after ensuring the relevant training status.

Sun Pharmaceutical Industries