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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 Executive - R&D (Molecular Diagnostics)- M.Sc in Biotechnology/Life Sciences / Microbiology

Join  R&D Team in Molecular Diagnostics
Erba Transasia is looking for passionate innovators to drive cutting-edge research in Molecular Diagnostics. 
 If you have a keen eye for detail and a desire to develop high-quality diagnostic solutions, this role is for you.
Details are Provided below 
1. Position: Executive - R&D (Molecular Diagnostics)
2. Location: Vizag
3. Qualification: M.Sc in Biotechnology/Life Sciences / Microbiology
4. Experience: 1 - 4 years in Molecular Diagnostics product development
5. Key Responsibilities:
• Extraction of nucleic acid from virus, bacteria and human samples • Standardization and optimization of molecular assays (PCR/qPCR)
• Calibration, verification and validation of developed assay
• Development of controls, standards and secondary reference material
• Development of protocol, procedure, SOP, IFU, work instructions related to the developed product
• Preparation of documents for regulatory approvals of developed assay
• To ensure smooth tech transfers and to establish good manufacturing practices and quality checks

Apply now 
Drop your resume at career@transasia.co.in and be a part of our talented R&D team. 
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