Assistant Manager- Production Pharma

Zentiva Poland; Ankleshwar; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Zentiva India is seeking an Assistant Manager – Production, Pharma to oversee monthly production planning with strict adherence to GMP, GQS and HSE standards. You will optimize resources and cycle times to meet customer needs. The role requires SAP expertise, leadership of a shift-based team of contractual staff and operators, and close coordination with Engineering, Quality and Maintenance to drive yield improvements and compliance.

Ideal candidates hold M. Pharma or B.

Qualifications

• Minimum 8–10 years in pharma primary/secondary packing.
• Exposure to granulation, compression and coating processes.

Responsibilities

• Plan and implement monthly production schedules with GMP/GQS/HSE compliance.
• Lead production activities in assigned areas to achieve 100% customer service.
• Perform SAP-related activities and coordinate with Engineering, Quality and Maintenance.
• Supervise a shift team including contractual staff and operators.
• Able to troubleshoot in SAP and ISO 14001 environments and ensure process documentation.

Skills

Production planning

Team leadership

GMP compliance

Regulatory adherence

Education

M. Pharm / B. Pharm

Tools

SAP

Job description

Job Title

Assistant Manager – Production, Pharma

Educational Qualification and Experience

M. Pharm / B. Pharm from a reputed university, having 8 to 10 years in the pharmaceutical Primary and secondary packing section, and also exposure in manufacturing in Granulation, compression, and Coating.

Responsibilities

• Production Implementing a monthly production schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilization of resources and optimum cycle time.
• Performing the production activities in assigned areas to achieve 100 % customer service.
• Performing the SAP-related activities.
• Able to handle a team consisting of Contractual persons, FTC & Operators in the allocated shift.
• Able to do troubleshooting in the allocated area ISO 14001 and SAP.
• Adhering to ISO 14001 activities and objectives in Pharma Mfg.
• Performing all the SAP-related activities as and when needed.
• Compliance Implementing and ensuring compliance with GQS, HSE, and ISO guidelines/standards and maintaining documentation for the same, including process validation and qualification.
• Coordinating with Engineering department for preventive and breakdown maintenance, modifications etc.
• The purchase department for procuring and controlling auxiliaries.
• Quality department for all quality-related matters.
• Packaging department for bulk availability.
• Yield monitoring Implementing and making efforts for the continuous improvement of the yield of assigned products.
• Training Impart training to the operative staff (like contractual persons, FTC & operators ) on GMP, Data Integrity ,HSE, ISO requirement & process improvement and maintaining good industrial relation in the plant by effective grievance process.
• Others 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 behavior and promptly reporting other potentially hazardous situations.
• Maintaining plant assets in good condition and making optimum use of all resources.
• Ready to work in each shift & in any allocated areas.

About the Company

At Zentiva, we provide health and wellbeing for all generations, with focus on developing, producing, and delivering high-quality, affordable medicines to more than 100 million people in over 40 countries across Europe. We have four manufacturing sites and a broad network of external manufacturing partners. Zentiva employs more than 5,400 unique talents in over 30 countries, bonded together by a commitment to the people who depend on our products every day. Visit us at www.zentiva.com