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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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Vacancy in Hetero Biopharma

Hetero Biopharma Recruitment 
Details are provided below 
1. Department- Analytical Development Lab ( R and D ) 
2. Qualifications - M. Tech. / B. Tech/ M Sc Biotechnology/ Biochemistry/ Any Life Sciences 
3. Experience- 2 to 4 Years 
4. Preferable- Biologics/ Injectables 
5. Job Location- Hetero Biopharma Ltd .Jadcherla Telangana 
6. Job Responsibilities- 
a. Development of mass Spectrometry based methods for analysis of various molecules, LC MS data generation for pivotal studies such as Biosimilarity , comparative studies 
b. Operations and maintenance of mass Spectrometry instrument and ancillary units . 
Routine monitoring of the instrument performance and assist in any troubleshooting activities. 
c. Developing and carrying out multiple assays aimed at Characterization of protein based therapeutics across various stages of the projects. 
d.  Participate in the design, development and implementation of methods for critical quality attributes Characterization of the molecule. Interpret results and draw conclusions from multistage experiments and note significant deviations, then suggest , design and pursue relevant experiment. 
e. Follow procedures and protocols, maintain accurate records, Lab note book and generate quality data for product development and analytical studies.
f. Collection and organization of technical data , author documents such SOP , MOA and reports necessary for product development and analytical studies. 
7. How to Apply- Interested Candidates are requested to send updated resume to manitej.s@hetero.com 
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