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The Associate is responsible for performing analytical chemistry research and/or development in collaboration with others to develop assays based on new and existing methodologies. Assist in developing and validating testing methodology used to control raw materials, in process materials, and final drug products. Conduct testing of analytical samples and/or GMP samples for the development of drug
Posted 2 months ago
Manages the quality control group related to the release, stability, drug product characterization, provable acceptable range studies, validation studies and other regulatory reportable testing activities. Responsible for the development, implementation and maintenance of quality control systems. Oversees development and implementation of standards, methods and procedures for inspecting, testing a
Posted 3 months ago
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