Zydus Cadila Walk-in Interview


About Company

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Zydus Cadila has rich experience in servicing large scale custom manufacturing needs of global customers in agrochemicals, pharmaceuticals, and specialty chemicals. Deccan’s business growth has been based on high quality, sustainable and safe production capability, affordable prices and proven track record of completing new projects on time. 

Zydus Cadila Walk-in Interview 2022 M. Tech/ B. Tech with Biotechnology, M.Sc. (Biotechnology)  for Manufacturing At Ahmedabad. Zydus Cadila Notification full details below. Interested and eligible candidates can Send Resume.

Vacancy details:

  • Post Name: Manufacturing
  • Qualification:   M. Tech/ B. Tech with Biotechnology, M.Sc. (Biotechnology)
  • Experienced:01-6Years

Job Description: Zydus Cadila Hiring For Manufacturing ! 

  • Important Details :
  • Location: Ahmedabad
  • Salary: ₹ 1,00,000 – 6,00,000 P.A.
  • Contact – Arvind Kumar Singh (08016095113)
  • Post of date:22/02/2022
  • Selection Process: The selection will be on the basis of Interview

Date & Time:27th February, 9.30 AM – 5.30 PM

Interview Venue :Hotel K C CROSS ROAD,Site No 1,Sec 10 ,Opp. Bus Stand Panchkula-134113(HARYANA).

Roles and Responsibilities

Manufacturing (Upstream Process):

Qualification: – M. Tech/ B. Tech with Biotechnology, M.Sc. (Biotechnology)

With 2-8 years of hands on experience of handling equipment such as fermentation Process, Automated fermenters, continuous centrifuges, filtration skids, Automated CIP & SIP units, Knowledge to perform aseptic handling, knowledge of GMP documentation. Must be familiar with cGMP requirements.

Manufacturing (Downstream Process):

Qualification: – M.Tech/B.Tech with Biotechnology, M.Sc. (Biotechnology) with 2-8 years experience in formulation & filling. Should be able to operate chromatography column (large volume), Automated TFF Systems, DS filtration activities inside B&C grade. Knowledge of media/buffer preparation & reagents as per defined system.

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Good Knowledge of QMS – GMP documentation.

Must be familiar with cGMP requirements.

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