Zydus Biologics (also known as Zydus Cadila) is an Indian multinational pharmaceutical company headquartered in Ahmedabad, Gujarat, India primarily engaged in the manufacture of generic drugs. It ranked 100th in the Fortune India 500 list in 2020. Cadila was founded in 1952 by Ramanbhai Patel (19252001), formerly a lecturer in the L.M. College of Pharmacy, and his business partner Indravadan Modi. It evolved over the next four decades into an established pharmaceutical company.
Join our team at Zydus Biologics (Zydus Biotech Park), Ahmedabad for Quality Assurance, Quality Control, Warehouse and Engineering
Quality Assurance
- Qual. M.Sc. Biotech / Biochemistry / Microbiology
- Exp. 3-7 years
- Section: IPQA, QMS, Analytical QA and Documentation Cell
Quality Control
- Qual. M.Sc. Micro / Biotech / Biochemistry
- Exp. 3-7 years
- Section: Microbiology, Chemical, RM/PM
Warehouse
- Qualification: Any Graduate / Post Graduate
- Exp. 3-5 yrs of exp. in Dispensing and Receipt of raw material, Packing Material, qualify cold chambers / cabinets & temperature mapping.
Instrumentation Engineer
- Qual. B. E/ B. Tech – Instrumentation
- Exp. 2-5 years
Engineering Plant Operator
- Qual. ITI/ Diploma Engineer
- Exp. 3-8 years
- Section: Water System, Electrician, HVAC
For all above positions, candidates having exposure to regulatory requirement of documentation, cGMP/GLP and SAP is essential.
If interested please share your CV at [email protected]
Inviting candidates for USP / DSP / QMS Production at Zydus Biologics (Zydus Biotech Park), Ahmedabad
- Qual. M.Sc. Biotech / B.Tech Biotech / M.Tech Biotech
- Exp. 2 – 12 years
USP Production:
- Executive/Senior Executive/ Assistant Manager: M.Sc./ B. Tech/B. E/ M. Tech – Biotechnology/Biochemistry with 3 – 10 years of experience in handling of large-scale mammalian cell culture (SS bioreactor), media/feed preparation and its filtration. The job requires readiness of bioreactor and associated vessels (CIP, FIT, PHT, SIP), operation of bioreactor & associated vessels, readiness and operation of centrifuge, clarification of cells for manufacturing of monoclonal antibodies/ bio therapeutic protein.
DSP Production:
- Executive/ Senior Executive/ Assistant Manager: M.Sc./B.Tech/ B. E/ M. Tech – Biotechnology/Biochemistry Candidates with 3-10 years of experience in downstream purification process for recombinant products, TFF system, chromatography system, virus filtration procedures and CIP/SIP of the equipment.
QMS Production:
- Executive/ Senior Executive/ Associate Manager: M.Sc./B.Tech/ B. E/ M. Tech – Biotechnology/Biochemistry Candidates with 3-15 years of experience in Preparation of risk assessment and investigation report. Meetings with cross functional team to identify the root causes of deviation, OOT and OOS. Initiation and/or review, closing of the QMS document such as deviation, change control and CAPA using Trackwise or similar software. Regular discussion with manufacturing team to reduce the human errors which leads to deviation. Preparation and/ or review of cGMP documents such as MFR, BMR, SOP etc.
For all above positions, candidates having exposure to regulatory requirement of documentation, cGMP/GLP and SAP is essential.
If interested please share your CV at [email protected]
