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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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Required Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing)

Aurigene Oncology Requires Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing) 

Details are provided below 
1. Post -  Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing) 
2. Qualification- M. Sc. ( Specialization in any Life Sciences) 
3. Experience-  2 to 13 Years 
4. Mandatory Skills- Candidate should be from vaccine or biosimilar background, experience in Upstream Manufacturing, handling Mammalian Cell Culture, QMS. 
5. Roles and Responsibilities 
a. Responsible for optimization of CAR cells Manufacturing processes using normal human or patient derived primary blood components following ethical practices and QMS as per GMP guidelines.  
b. Actively engage in the manufacture of CAR - T cell Therapy products by diligently prioritizing the lab functions to meet critical deadlines 
c. Establish and carefully execute transductions by viral vector and non viral vector based approaches, activation and expansion of immune cells ( T cells , NK cells etc ) isolated from Clinical specimens without compromising sterility and Quality parameters as per the guidelines and defined criteria by maintaining highest standards and assist in technical transfer and core R and D activities.  
d.  To review and document SOPs , Protocols and reports pertaining to the program requirements.  
e. Work with vendors to evaluate raw materials and consumables for compatibility with the manufacturing processes. 
f. Prepare for and participate  in the compliance monitoring inspections/regulatory agency interactions. 
6. How to Apply- Interested Candidates may share their resume to gayathiri_n@aurigene.com 

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