Zydus Biologics is hiring in Production (USP / DSP) / QA (IPQA / Validation).Zydus Biologics, a super-specialty centric business entity of Cadila healthcare Ltd., is engaged in manufacturing and commercialization of both, small molecule, biological drugs and vaccines intended for prevention and treatment of various diseases in the field of oncology, hepatology, nephrology, rheumatology.Application form link provided at the end of post.
Walk in Details :
- Company Name: Zydus Biologics
- Location :Ahmedabad
- Post Name: Production (USP / DSP) / QA (IPQA / Validation)
- Qualification: M.Sc.(Biotechnology)/B. Pharm / M.Pharm,B.Tech Biotechnology / B.E Biotechnology
- Experience: 03 -07 Years
- No of Vacancies: Details not provided by recruiter
- Details of Salary: Details not provided by recruiter
- Contact: Ruchi.firstname.lastname@example.org
- Selection Process: Based on interview
Job Description/Skills Required.
Opening in Zydus Biologics for USP/DSP Production and QA – IPQA/Validation Department based at Zydus Biotech Park, Ahmedabad
Executive / Senior Executive / Assistant Manager
For Production we are looking for B.Tech Biotechnology / B.E Biotechnology / M.Sc. Biotechnology / M.Sc. Microbiology with 3 to 7 years of hands on experience on CIP/SIP of the equipment, Fermenters, Process vessels, Centrifuge, TFF system, LAF, Shaker incubators, Chromatography system, Cold rooms and freezers for below mentioned openings:
Production – Upstream Processing – Code: USP
Responsible for handling bacterial fermentation process, continuous centrifuge, 1 kl – 5 kl fermenters, shaker incubator.
Production – Downstream Processing – Code: DSP
Responsible for downstream purification process for recombinant products, handling of equipment such as TFF system, chromatography system, depth filtration procedures.
QA-Validation – Code: Validation we are looking for M.Sc.(Biotechnology)/B. Pharm / M.Pharm with 5 to 7 years of hands on experience in Equipment Qualifications (Fermenter, Bioreactor, Media/buffer preparation Vessels, Autoclave etc.), Utility Qualifications, HVAC, Water System, Protocol preparation and its compilations. Should be responsible for Media fill activities, protocol & BMR preparation/review.
QA Oversight manufacturing – Code: IPQA
Should be responsible for QA Oversight (IPQA) related activities for Drug substance manufacturing along with handling of process validations, cleaning validations OOS, change control, deviation, investigation, CAPA and QMS activities.
For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP is essential.
Interested candidates may send their updated CVs along with Total exp., Notice Period, current and expected CTC to email@example.com by on or before 30/07/21