Zydus Biologics – Urgent Openings for Production & Quality Control @ Ahmedabad
We invite candidates for Executive/Sr. Executive/Asst. Manager positions of Production and Quality Control department based at Zydus Biologics, Biotech Park, Ahmedabad
Production (Downstream Processing)/Upstream Processing):
MSc. Biotechnology / Biochemistry, B.Tech/ M. Tech with Biotechnology / Biochemistry / Biochemical engineering with 2-8 years of hands on experience in following operations of Down Stream / Upstream Process
Production (Down Stream Processing): Code 01
Responsible for Operation of chromatography system, Operation of TFF system, CIP/SIP of equipment used for DSP, Preparation and execution of GMP documents and Knowledge about QMS
Production (Upstream Processing): Code 02
Responsible for Cell culture activities for seed development, Operation of bioreactor, Isolation of cells using centrifuge and depth filtration, CIP/SIP of equipment used for upstream process, Preparation and execution of GMP documents, Knowledge about QMS
Quality Control (Protein analytics)/(Bio assay): Code 03
MSc./B.Sc (Biotechnology / Biochemistry / Microbiology / Chemistry) with 2-8 years of hands on experience of handling equipment & tests such as HPLC/UPLC, CZE, UV Spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA, Bioassay, microbial identification, GC, IR, KF auto titrator, coulometer, melting points, handling stability studies and GMP documentation.
For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential.
Interested candidates can send their updated CV by mentioning the Code no. to Ruchi.firstname.lastname@example.org
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