BSV Production Exec Job
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BSV Production Exec Job For BTech, MSc Biotech, Microbiology, Biochem Candidates

BSV Production Exec Job For BTech, MSc Biotech, Microbiology, Biochem Candidates. BSV job opening for BTech, MSc Biochem, Microbiology and Biotechnology job openings. Interested and eligible applicants can check out all of the details on the same below

Hey there, looking for some interview questions and the answers for the role of Production Executive (Biotech API) at Bharat Serums and Vaccines (BSV), then check them out below


Experience: From 5 to 8 year(s) of experience

Location: Ambernath

About the job

About BSV:

For over five decades, we at BSV have used scientific resources to develop a range of biological, biotech and pharmaceutical products. We want to be a leading biopharmaceutical company driven by people and science to set benchmarks in patient outcomes across therapy areas of Women’s Health, Critical Care and Emergency Medicine.

Roles and Responsibilities:

  1. Maintaining all equipment/machines in consultation with the maintenance department.
  2. Maintaining the flow of material as per man & material movements.
  3. Maintaining availabilities of spares/change parts required for equipment/machines located in the department in consultation with the Maintenance department.
  4. Responsible for the operation, and cleaning of STR and wave bioreactor & operation and cleaning of chromatography system and related equipment.
  5. Responsible for calibration of instruments & maintenance of status labels of instruments, equipment and area.
  6. Monitoring of area cleaning and maintenance as per cGMP requirements.
  7. Responsible to fulfill the operational requirements of the area as per cGMP requirements.
  8. Issue & receipt of raw materials from stores required for batch operation as per the BMR process.
  9. Responsible for proper gowning & change as per relevant SOP.
  10. Maintaining the flow of material as per man & material movements.
  11. Execution of batches as per BMR.
  12. Filling of logs and BMR & other cGMP documents as per requirement.
  13. Reviewing SOPS of all activities of the line.
  14. Responsible to perform pre-operational checks and line clearance from Q.A. prior to each operation.
  15. Reporting any abnormal observation to the superior during operation.
  16. Responsible for various water rinse samples of cleaned equipment as per requirement.
  17. To understand and follow the company’s environmental health and safety policy.
  18. To follow Safety Rules and Standard Operating Procedures at the workplace.
  19. Participate in environment, health and safety training and awareness programmes.
  20. To understand the SOP of relevant machinery, tools, substances, etc. before use.
  21. Use of essential Personal Protective Equipment at the workplace.
  22. Report any abnormalities, near-miss incidents, unsafe acts & conditions in the workplace, equipment, etc. which might endanger the environment, health and safety to the respective departmental EHS coordinator or EHS department.

Key Skills

  • Production
  • GMP
  • API Manufacturing
  • Compliance

Skills that are made bold are preferred key skills


  • UG: B.Tech/B.E. in Bio-Chemistry/Bio-Technology
  • PG: MS/M.Sc(Science) in Biotechnology, Microbiology

Role: Production & Manufacturing – Other

Salary: Not Disclosed by Recruiter

Industry: Pharmaceutical & Life Sciences

Department:  Production, Manufacturing & Engineering

Role Category: Production & Manufacturing – Other

Employment Type: Full-Time, Permanent


Hey there, looking for some interview questions and the answers for the role of Production Executive (Biotech API) at Bharat Serums and Vaccines (BSV), then check them out below

  1. Can you describe your experience in API manufacturing and your role as a Production Executive? Answer: In my previous role as a Production Executive, I had 5 years of experience in API manufacturing. My responsibilities included maintaining equipment, ensuring the flow of materials, operating and cleaning bioreactors and chromatography systems, calibrating instruments, maintaining cleanliness and adherence to cGMP requirements, executing batches as per BMR, and documenting activities in logs and BMRs.
  2. How do you ensure compliance with GMP (Good Manufacturing Practices) in your day-to-day work? Answer: Compliance with GMP is crucial in pharmaceutical manufacturing. I ensure compliance by strictly following SOPs, maintaining cleanliness and hygiene standards, adhering to equipment calibration and maintenance procedures, documenting activities accurately, and participating in regular training and awareness programs related to environment, health, and safety.
  3. Can you share an example of a challenging situation you faced in API manufacturing and how you resolved it while maintaining quality and efficiency? Answer: One challenging situation I encountered was when a critical piece of equipment malfunctioned during a batch operation. To resolve the issue, I immediately informed the maintenance department, followed the standard operating procedures for troubleshooting, and collaborated with the technical team to find a temporary solution while the equipment was being repaired. We ensured that the quality of the batch was not compromised and maintained efficient production by adjusting the workflow accordingly.
  4. How do you prioritize tasks and manage multiple production activities simultaneously? Answer: To prioritize tasks and manage multiple activities, I rely on effective communication and coordination with the team members. I assess the urgency and criticality of each task, plan and allocate resources accordingly, and constantly monitor the progress. By staying organized, setting clear priorities, and adapting to changing requirements, I ensure smooth operations and timely completion of production activities.
  5. In your experience, how have you contributed to the continuous improvement and optimization of production processes in API manufacturing? Answer: As a Production Executive, I actively participated in process improvement initiatives. I regularly reviewed SOPs, identified areas for optimization, and suggested process modifications to enhance efficiency and reduce waste. I also collaborated with cross-functional teams to implement lean manufacturing principles, such as 5S and waste reduction techniques, resulting in improved productivity and cost savings.

Note: The answers provided are examples and should be tailored based on the candidate’s specific experience and achievements in API manufacturing.

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