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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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Jubilant Generics Limited requires Executive/officer

Jubilant Generics Limited are looking for a dynamic candidate to join 

Company: Jubilant Generics Limited, Roorkee

Position: Executive/officer - MSTG Technology Transfer
Experiences: 3 to 8 years
Qualification: B. Pharm/M. Pharm
Location: Roorkee (Uttarakhand)
Job Description:
  • Responsible for preparation of PPQ protocol/report/Scale up protocol/report
  • Responsible for preparation of qualitative and quantitative risk assessment for change in batch size/equipment etc.
  • Responsible for preparation of stability protocol
  • Responsible for preparation of Hold time study protocol and its Summary Report.
  • Tracking the outcome of CAPA of Deviation/OOS/OOT and completed within predefined time in CAPA Track wise.
  • Responsible for preparation of batch record
  • Responsible for continuous improvements in the commercial products at site to improve the efficiency, productivity, delivery and safety resulting in effective and efficient operation.
  • Handing of QMS documents such as deviation/ OOS/OOT/ Investigation/Market complaints.
  • Initiate the CCR accord to production plan.
Interested candidates can share their resume at varnika.chaudhary@jubl.com
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