DivisionIPDDepartmentIPDEmployment TypePermanentJob PurposeExecute the core method development activities and conduct analysis of routine as well as stability samples to finalize specifications and ensure timely delivery of product to unitAccountabilitiesI. Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators
II. Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation
III. Document and interpret the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms
IV. Provide support to units or CFTs for transfer of analytical methods and techniques by visiting and demonstrating them with the relevant analysis to ensure successful and timely transfer of products
V. Maintain proper safety, GLP, and GMP environment in the work place to minimize accidents and incidents
VI. Review the analytical requirements and recommend corrections in specifications by coordinating with units and CFTs to ensure smooth operationsEducation QualificationM. Sc. (Analytical Chemistry) / M. PharmRelevant Work Experience2-4 years of experience in pharmaceutical organisation with knowledge of handling instruments like HPLC, GC, Dissolution tester and DPI related instrumentsCompetencies/SkillsCollaborate to SucceedInnovate to ExcelPerform with AccountabilityLead with EmpathyAct with AgilityStrong Domain KnowledgePeople ManagementJob LocationVikhroliShift Hours
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