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Required Drug Substance (Viral Vaccine Experience)- Upstream /Downstream Processing of viral vaccines

Job Opportunity - Drug Substance (Viral Vaccine Experience) Bharat Biotech is looking for skilled professionals with hands-on experience in Drug Substance manufacturing for Viral Vaccines. Details are provided below  1. Location: Hyderabad 2. Experience: 2-6 Years 3. Key Skills & Experience Required a. Experience in Upstream /Downstream Processing of viral vaccines b. Operation and handling of bioreactors, fermenters, centrifuges, chromatography systems, filtration units c.  Knowledge of cell culture techniques (mammalian/avian cell lines)  d. Familiarity with aseptic techniques, GMP documentation, batch records e. Understanding of process optimization, scale-up, and technology transfer f. Exposure to in-process testing, troubleshooting, and equipment cleaning/sterilization g. Ability to work in a regulated, fast-paced manufacturing environment 4. How to Apply Interested candidates can share their updated CV to kiran4978@bharatbiotech.com Mention subject line as: Appl...
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Requirement of Senior Executive for Upstream in Classical Fermentation bulk Production for API Pharma.

Hiring  For Upstream Department


Candidate required for Upstream in Classical Fermentation bulk Production for API Pharma.
Designation – Senior Executive
Experience – 8+ Years
Qualification – B.Tech/M.sc/B.sc (Biotechnology)
Location - Pithampur - SEZ

Responsibilities:

1. Preparing, reviewing and approving the instruction for the production of intermediates and APIs according to written procedure.
2. Production of APIs and intermediates according to pre-approved instruction.
3. Reviewing all production batch records ensuring these are completed and signed.
4. Ensure that the production deviations are reported and evaluated, Critical deviation are investigated and conclusions to be recorded.
5. Ensure that the production facilities are clean and ensure schedule of cleaning
6. Ensure that the necessary calibration is performed and records kept.
7. Ensure that validation protocols and reports are reviewed and approved.
8. Ensure that the premises and equipment are maintained, and records kept.
9. Evaluating proposed changes in product, process and equipment.
10. To ensure the implementation of changes as per the assessment and action identified.
11. To ensure reporting of all production related deviation.
12. To perform investigation of deviation.
13. To review the risk assessment.
14. To assist in department level SOP Preparation.
15. Ensure that new, modified facilities and equipment are qualified
16. To ensure congenial and safe work environment.
17. Identify training need for the department personnel and provide the same as per schedule.
18. Responsible for synchronization of production and sales plan thereby to meet the annual sales target for API and intermediate.

Interested candidate share your cv at: Pratiksha.dubey@symbiotec.in

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