B.Tech

RM, PM, FG, Dispensing, Dispatch, Documentation. After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines

Ensure that Bulk Viral Antigen production adheres to GMP standards on the shop floor, including line clearance, dispensing, and preparation processes. Examining and approving batch records, standard operating procedures, project plans, customer verification, and APS documents.

First Class Masters degree in Molecular Biology or Biotechnology, Medical Biochemistry, Applied Biology, Life Sciences from a recognized university with 4 years of experience in relevant area.

M.Sc./ M.Tech./ M.Pharm./ B.Tech. or equivalent in Biotechnology and allied areas; Research project entitled Targeting Autophagy and Microtubule Dynamics for Next- Generation Cancer and Neurovegetative Disease Treatment funded by Gujarat State Biotechnology Mission, Govt. of Gujarat.

Doctoral Degree in Science, Engineering, Technology, Pharma, MD, MS from a recognised University or equivalent.

Candidates with B.E, B.Tech degree in Chemical Engineering, Biotechnology, Chemical Techology or M. Sc. Chemistry, Biochemistry or B.Pharma from a recognized university, institute with Mathematics at 10+2 level. Final Year students can also apply for the program.

M.Sc in Organic Chemistry, Pharmaceutical Chemistry Or M.Pharm, M.S Pharm in Medicinal Chemistry. Minimum one year hands on experience in organic synthesis.

Masters degree in Microbiology, Biotechnology, Chemical Engineering, Natural, Agricultural Sciences, MVSc or bachlors degree in Engineering or Technology or Medicine from a recognized University