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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

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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Biological E. Limited is hiring for Multiple Positions

Biological E. Limited is hiring for Multiple Positions
Position: Assistant Manager/ Deputy Manager
Qualification: M. Sc. (Life Sciences )/B. Tech.  /M.Tech  (Biotechnology)
Experience: 08- 12 years
Job Responsibilities:
  • Expertise in any bacterial/viral vaccine development or manufacturing process.
  • Experience in In-process Quality assurance/R&D/MSAT departments of a vaccine manufacturing company.
  • Knowledge on QBD Concept, design space, scientific experimentation, risk assessment, and statistical analysis.
  • Understanding of pharmacopoeial requirements, WHO TRS and other applicable guidance documents.
  • Experience on handling Deviations, change control and OOS.
  • Knowledge on cell/viral bank system and maintenance.
  • Knowledge on Review & Approval of Protocols (PV, CV etc), study reports, BPRs, MFRs and SOPs.
  • Hands on experience on cleaning validation and process validation.
  • Hands on experience with preparation of Product Development Reports/SOP/BPR/MFR /Protocol and its review.
  • Experience in Technology transfer between Internal or external facilities.
  • Must have handled regulatory inspections from WHO, FDA or EMA.
No Gender Bias. 
Only candidates having relevant experience can send their share resume at sthitapragnya.nayak@biologicale.com
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