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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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Syenergen Bio Private Limited Requires Research Associate ( Report Writers ) - B. Pharm, M. Pharm. M Sc.

Syenergen Bio Private Limited Requires Research Associate ( Report Writers ) - B. Pharm, M. Pharm. M Sc. 
Details are provided below 
1. Post - Research Associate ( Report Writers) 
2. Company- Synergen Bio Private Limited Pune 
3. Department- Project Management and Biopharmaceutics 
4. Qualification- B  Pharm,  M. Pharm, M. Sc. 
5. No. Of Vacancies 02 
6. Experience- 1.5 + Years 
7. Note - Immediate Joiners preferred 
8. Job Location- Shivajinagar , Wakdewadi , Pune 
9. Tasks Responsibilities- 
a. Preparation of Clinical Study Report ( CSR) within proposed time line according to raw data and as per the regulatory requirements.  
b. Preparation of electronic copy of final reports ( scanning , book marking , hypertext linking , inherit zoom and creating TOC to PDFs 
c. Know about eCTD specifications guidelines for regulatory submissions 
d.  Coordination with Clinical, Bioanalytical department and principal and investigators while preparation of Clinical Study Report and compilation of data .
e. Data uploading ( demographies, Clinical laboratory values , vital signs , meal distribution, and Deviation of sample time point.) 
f. Preparation of relevant report appendices as per project.  
g. Coordinating with different sections with projects related activities.  
h. Preparation of regulatory summary reports in Module 02 and clinical study reports in Module 05( i e. eCTD Format) 
10. Interested candidates share CV on careers@synergenbio.com 
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