Home Head/VP/CEO/President/GM Lead (Head) Production | Emcure Pharmaceuticals | Kurkumb, Pune

Lead (Head) Production | Emcure Pharmaceuticals | Kurkumb, Pune


Emcure is the 12th Largest pharmaceuticals company with 10000+ employees spread across 70+ countries with 15 subsidiaries and 7 representative offices producing 800+ products across various therapeutic categories.

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Position: Lead Production

Location: Kurkumba, Pune, Maharashtra, India

Job Description:

Objective: Department Head, responsible for all production department related activity.

Responsible for API-1, API-2, and API-7 plant manufacturing operations.

  • Prepare monthly production planning as per the designed and standard system.


  • To give the responses against self-inspection, customer, regulatory, safety, and compliance system audit and assist to QA department for customer complaints.


  • To evaluate proposed changes in product, process, or equipment.


  • To monitor scale up / trials and validation of new molecules and existing product with the R&D department.


  • To ensure that GMP practices and safety procedures are followed in plant.


  • To verify miscellaneous protocol base activity performed as per requirement through QMS.


  • To initiate / authorization for necessary modification and changes through change control system.


  • Continuous improvement with respect to system, Atomization, Quality, and cost.


  • To minimize failure rates and COPQ (Cost of poor quality).


  • Production planning and deliveries as per internal and external customer satisfaction.


  • To ensure measures in place for inventory control.


  • To give suggestions with reference to the technical concepts.


  • To improve productivity by improving batch size and reduction in the time cycle with proper documentation.


  • To ensure training (cGMP awareness and related training of employee has completed) and all the products are manufactured with standards.


  • Ensuring schedule adherence with respect to VMP (Validation master plan) Calibration, Qualification, and Preventive maintenance.


  • Review and Verified of all cGMP documents like change control and supporting documents, SOP, Incident, Deviation, LIR and Investigation reports, and CAPA.


  • To optimize assets utilization.


  • To ensure the work permit system is followed in the department.


  • To carry out Track wise related activity.


  • Making sure that production facilities are clean and when appropriate disinfected.


  • Making sure that new and, when appropriate, modified facilities and equipment are qualified.


  • Making sure that the premises and equipment are maintained.


  • Is authorized to sign as “Department Head” in department related documents as per the requirement.


  • As per the requirement, can do the authorized sign as “Site Head / Designee” on related documents.

Qualification: B.Tech/B.E Chemical

Experience: Minimum 20 Years

Contact Details:


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