Executive, Production - Pharmaceuticals

Implementing and ensuring compliance with GMP, HSE, and ISO guidelines/standards in assigned production areas.

Maintaining GMP documentation for the process as well as area documents in assigned production areas.

Maintaining documentation for the process validation and qualification in assigned production areas as and when needed.

Collaborate with the Quality Assurance (QA) team to implement and maintain quality control measures.

Coordinating with…

Shift reliever for day-to-day activities on the shop floor in assigned production areas.

Engineering department for preventive and breakdown maintenance, modifications, etc.

Quality department for all quality-related activities related to assigned production areas.

Warehouse department for any materials supply.

Monitoring and improving the yield of assigned products.

Monitoring and improving the overall equipment efficiency of the respective area.

Maintain the standard labour hours of respective products.

Monitoring and improving the on-time in full delivery.

Impart training to the operative staff on GMP, HSE, ISO requirement, operation of machines and process improvement.

Participate in root cause analysis and problem-solving initiatives to address production challenges.

Report any equipment malfunctions or breakdowns to ensure timely repairs and minimal production downtime.

Carrying out any other assignments or projects like qualifications and validations as per the instruction of the dept. Head to meet the organizational priorities.

Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.

Maintaining plant assets in good condition and making optimum use of all resources.

Zentiva Group Values :

Accountability, Authenticity, Collaboration, Courage, Trust