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

Required Scientist-B(Fermentation)-M.Sc/M.TechBiotechnology, Microbiology, Biochemistry or Molecular Biology

Privi Biotechnologies Pvt. Ltd. is looking for an experienced fermentation scientist to independently lead pilot plant scale-up operations. Details are Provided below   1. Designation: Scientist-B (Fermentation) 2. Location: Nerul, Navi Mumbai 3. Qualification: M.Sc/M.Tech Biotechnology, Microbiology, Biochemistry or Molecular Biology 4. Experience: 4-6 Years 5. Reporting to: Deputy Manager 6. Key Responsibilities: -Execute bench-to-pilot scale-up, experimental and validation batches -Optimize process parameters and troubleshoot batch/process variations -Ensure execution of SOPs, process instructions and safety procedures Prepare and maintain BMRs, batch sheets. SOPs and equipment logbooks -Coordinate raw materials, CIP/SIP, cleaning and line-clearance activities -Monitor equipment, coordinate maintenance, and supervise trainees/operators 7. Key Skills: -Microbiology techniques distillation, microfiltration, chromatography -Hands-on fermenter handling (R&D and pilot...
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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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