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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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Virchow Biotech Pvt Ltd Requires Jr. Executive To Sr Executive for QMS, IPQA, Validation Department- Total 60 Vacancies

Virchow Biotech Pvt Ltd Requires Jr. Executive To Sr  Executive for QMS, IPQA, Validation Department- Total 60 Vacancies
Walk In For Quality Assurance- QMS, IPQA, Validation 

Details are provided below 

1. Designation - Jr.Executive To Sr Executive 
2. Department- Quality Assurance ( QMS, IPQA, Validation) 
3. No. Of Vacancies- 60 
4. Qualification- M. Pharmacy,  B. Pharmacy  OR M. Sc. Or B. Sc. ( Life Sciences) 
5. Experience- 2 to 8 Years 
6. Budget - Based on their present CTC 
7. Job Description 
a. Oversee the development, implementation and maintenance of the Quality Management System within the Probiotics or non aseptic manufacturing facility . This includes ensuring that all processes  , procedures and documentation comply with the relevant regulatory standards such as Good Manufacturing Practices ( GMP) 
b. Manage change controls, deviations and incidents by collaborating with stakeholders ensuring proper closure upon execution 
c. Should take plant round for monitoring of entire production operations and confirm quality conformance to specifications. 
d. Should check documents like equipment logbooks, temperature and humidity records 
e. Collect in process and finished samples as per specifications and protocols. 
f. Supervision of RM / PM sampling and dispensing procedures. 
g. Machine line clearance of production area. 
10. Interested candidates can share their CV with the below mentioned mail id raghu@virchowbiotech.com , hirings@virchowbiotech.com 

Note - For Interview Date, venue and date and time please check the image.  
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