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Tianish Laboratories in Hyderabad invites applications for analytical development roles focused on HPLC method development and validation. The role emphasizes documentation, coordination with CRD, DQA, CQA to harmonize specifications, and adherence to GLP and safety practices.
The preferred candidate holds an MSc or MPharm with 2–5 years of experience in ARD - Method Development and Method Validation at our R&D Centre, Hyderabad.
Qualification: Master of Science/Master of Pharmacy
Experience: 2 - 5 Years
Department: ARD - Method Development, Method Validation
Location: Hyderabad, R&D Centre