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In combination with QA Document Control and QA GMP Manufacturing leads, help manage Documentation Management for Pharmaceutical, Analytical, Formulation Process Development, and corresponding cGMP activities.
$145,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Key Responsibilities:Document all experiments and results thoroughly with detailed observationsExercise technical discretion in the design, execution and interpretation of experiments that contribute to project strategies and goalsPerform method development and validation activities in an GMP environment.
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RESPONSIBILITIES:o Work in a fast-paced GMP environment performing testing using various analytical techniques, such as HPLC, Dissolution, GC, PXRD, FT-IR, DSC, and KF.o Record and report results of analysis in accordance with lab procedures, GDP, and ALCOA.o Review and interpret analytical test results.
$40 depends on experienceFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Maintains a robust training matrix within the LMS for all GMP related training. Manages the annual GMP Training program and ensures that all staff comply with training requirements. The Quality Assurance team with Serán BioScience is seeking a Training Administrator to support the education and abilities throughout our GMP workforce.
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GMP Materials Specialist. Team-oriented environment with responsibilities that include both domestic and international shipping. Aerotek is an Allegis Group company, the global leader in talent solutions.
Full-timeExpandApply NowActive JobUpdated 2 days ago
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