BSc & MSc Biology, Biotech Candidates With 0-3 Yrs Exp Can Apply at Promea For An Executive Post

Promea Executive Vacancy For 0-3 Yrs Exp BSc, MSc Biology & Biotech, Apply Online

Promea Executive Vacancy For 0-3 Yrs Exp BSc, MSc Biology & Biotech, Apply Online. Promea IVD Rapids Production – Executive job opening for BSc, MSc Biology and Biotechnology candidates. Interested and eligible applicants can check out all of the details on the same below

Hey there, looking for assistance with possible interview questions and answers for the role of an executive at Promea? Then check them below

IVD ELISA Production – Executive

FULL-TIME

HYDERABAD

0 – 3 YEARS

We are seeking an Executive to Join our IVD ELISA – Production team. You will be planning and co-ordinating the production of ELISA HIV, Hepatitis B, and Hepatitis C kits at our facility.

Your responsibilities: 

• Planning and Coordinating for manufacturing of Rapids kits
• Documentation of BMR and BPR’s
• Supervising the casual Manpower and assigning work to complete on a timely basis.
• Material Management
• Equipment Maintenance / Calibrations

Skill Sets/Experience:

• Knowledge in IVD ELISA production
• Knowledge in Documentation
• Basic GMP awareness

Qualifications: 

• B.Sc, M.Sc – Biotechnology, Chemistry, Biology
• 0 to 3 Years experience in IVD industry

Job Type: Permanent, On-site

APPLY ONLINE

Hey there, looking for assistance with possible interview questions and answers for the role of an executive at Promea? Then check them below

1. Can you describe your experience with planning and coordinating the production of ELISA kits for HIV, Hepatitis B, and Hepatitis C? How did you ensure efficient and timely manufacturing? Answer: In my previous role, I was responsible for planning and coordinating the production of ELISA kits. I utilized production schedules, monitored inventory levels, and collaborated with cross-functional teams to ensure smooth operations. Regular communication and proactive problem-solving helped me meet production timelines effectively.
2. How familiar are you with the documentation requirements in IVD ELISA production? Can you provide an example of a document you have prepared or managed? Answer: I have a strong understanding of documentation in IVD ELISA production. For instance, I have experience in preparing Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs) to ensure accurate and consistent manufacturing processes. I have also maintained other relevant documents such as SOPs and equipment calibration records.
3. In this role, you will be supervising casual manpower. How do you ensure that work is assigned and completed on time? Can you share an example of how you handled a challenging situation with casual manpower? Answer: To ensure timely completion of work, I believe in effective communication and task delegation. By clearly communicating expectations, providing proper training, and offering guidance, I motivate casual manpower to perform their tasks efficiently. In a challenging situation, I proactively addressed any issues, provided necessary support, and reassigned tasks when needed to maintain productivity levels.
4. How do you manage material management in the production process? Can you discuss your experience with inventory control and ensuring the availability of materials? Answer: I am experienced in managing material requirements for production. By closely monitoring inventory levels, conducting regular audits, and working closely with procurement teams, I ensure the availability of materials while minimizing excess stock. I also prioritize communication with suppliers to maintain a smooth supply chain and address any potential delays or shortages.
5. Can you explain your understanding of Good Manufacturing Practices (GMP) in the context of IVD ELISA production? How have you implemented GMP guidelines in your previous role? Answer: Good Manufacturing Practices (GMP) are essential for maintaining quality standards in IVD production. I am well-versed in GMP requirements and have consistently implemented them in my previous role. This includes following standard operating procedures (SOPs), ensuring proper documentation and record-keeping, conducting regular equipment calibrations, and adhering to cleanliness and hygiene standards. I understand the importance of GMP in ensuring the safety and efficacy of the final products.

Remember, these questions are just examples, and you can adapt them based on the specific requirements and context of the role.

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