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In this role you are required to do analysis and solving of moderately complex problems

Proven ability to follow instructions and guidelines, work independently, and take initiative. Excellent attention to detail and accuracy in maintaining high-quality standards.

Support system implementation, upgrades, and change management. Work with clients and crosse Functional teams to ensure regulatory compliance 

Ensure the report is prepared as per the respective regulatory and sponsor requirements. Handle sponsors or regulatory queries on lab reports.

M.Sc. in Life Sciences, Biotechnology, Molecular Biology, Clinical Research, M.Pharm, Pharm.D or a related field

Candidate should have knowledge of IPQA, Validation, QMS. Responsible to adherence cGMP guidelines 

Cadila Pharmaceuticals is an Indian multinational pharmaceutical company based in Ahmedabad.

Roche has established Global Analytics and Technology Center of Excellence (GATE) at Chennai and Hyderabad to drive analytics & technology driven solutions by partnering with Roche affiliates across the globe

Perform analysis of ointment, cream, gel, solution, raw material, and stability samples. Hands-on experience with HPLC, UPLC, GC, UV, IR, pH, viscosity, and assay testing.