Location
In office (Ankleshwar)
Employment
Full-Time
Confirmed on the employer's own hiring board on Oct 28, 2026. First seen by Alion on Aug 24, 2026. Zentiva scores B on the Alion truth index.
Overview
Company
Impact
Profile match
Zentiva is a prominent European pharmaceutical enterprise specializing in the production and supply of high-quality generic medicines and consumer healthcare products. Headquartered in Prague, Czech Republic, the company operates across dozens of international markets, delivering accessible treatments to millions of patients. Managing the complete lifecycle from laboratory research and manufacturing to global distribution, it focuses on expanding access to affordable, essential medications.
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.
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.
Coordination
- 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
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