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Location
In office (India)
Employment
Full-Time
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 - Executive - Production, Pharma

Experience

1 to 5 years in pharmaceutical manufacturing (Preferably in Packing )

Education

B.Pharm (Bachelor of Pharmacy) , M.Pharm (Master of Pharmacy)

Key Accountability

Production

Implementing 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 in order to achieve 100 % customer service.

Performing the SAP related activities

Able to handle the team consist of Contractual persons ,FTC & Operators in 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 to 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 break down maintenance, modifications etc.
  • Purchase department for procuring and controlling auxiliaries.
  • Quality department for all quality related matters.
  • Production department for bulk availability.

Yield monitoring

Implementing and making efforts for continuous improvement of 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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