Home / Job / Zydus Biologics – Openings for Production (USP / DSP) / QA (IPQA / Validation) Departments

Zydus Biologics – Openings for Production (USP / DSP) / QA (IPQA / Validation) Departments

Zydus Biologics – Openings for Production (USP / DSP) / QA (IPQA / Validation) Departments

WALK - IN INTERVIEW For Zydus Biologics, Biotech Park Ahmedabad -

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 protected] by on or before 30/07/21

Apply for this position

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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