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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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Puerto Life Sciences Private Limited Requires Executives and Officers - B. Pharma / M. Pharma / M. Sc. ( Microbiology/ Chemistry/Biotechnology)

Puerto Life Sciences Private Limited , Neemrana , Rajasthan ( Sterile Faculty) Requires  Executives and Officers - B. Pharma / M. Pharma / M. Sc. ( Microbiology/ Chemistry/Biotechnology) 

Details are provided below 
1. Department- Production 
2. Skills Required With Experience of 1 to 5 Years for Sterile Manufacturing 
a. Experience in Sterile compounding processes including CIP/SIP Systems,Component preparation and sterilization.  
b.  Hands on experince in aseptic operations, media filling , sterilization processes and area monitoring.  
c. Ability to troubleshoot and manage challenges in aseptic manufacturing environments.  

1. Department- Quality Assurance 
2. Skills Required With Experience of 1 to 5 Years for Sterile Manufacturing 
a. Expertise in risk assessment , investigations, CAPA implementation and effectiveness checks 
b.  Through knowledge of SOPs , change control and compliance monitoring for Sterile environment
c. Strong understanding of batch record reviews , protocol preparation and regulatory compliance. 
d.  Proficient in handling deviations, internal / External audits, and ensuring GMP adherence in Sterile conditions. 
e. Experience in MQA operations and global sterilization standards verification 

1. Department- Quality Control 
2. Skills Required With Experience of 1 to 5 Years for Sterile Manufacturing 
a. Strong understanding of both analytical and Microbiological testing in Sterile Manufacturing. 
b.  Proficiency in Analytical Testing techniques ( HPLC, GC , UV etc ) for product quality and regulatory compliance. 
c. Expertise in Environmental Monitoring (variable/ non variable) Bioburden and Sterility Testing,
d.  Knowledge of stability studies , release  testing  and Pharmacopoeial requirements for Sterile products. 

Please share the required details such as  your resume, current CTC , and notice Period at hr@puerto.in CLICK HERE FOR DETAILS

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