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Forms cross-functional alliances with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs, Quality Control and Manufacturing Operations by providing SMEs to these functions and project teams.
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The VP of Drug Safety and Pharmacovigilance will provide the leadership and management for the infrastructure of the Drug Safety and Pharmacovigilance department across both clinical development and commercial products for the company.
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Proven experience in the integration and management of PDM, and PLM systems for the product development life cycle within a manufacturing or engineering environment. , ECO process, product structure, configuration engineering, change management, and revision control and tracking.
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Job Description POSITION SUMMARY The Director, Project Management is responsible for managing cross-functional drug development projects, in either preclinical or clinical development stages.
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Participate in new feature and automation development, write unit test, self test and QA software, continuously deliver high quality engineering results. Partner closely with our product managers, engineers, product designers, and key business leaders to improve the overall self-serve rate of our Chatbot.
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Reports to: Associate Director, Analytical Development. Extensive expertise in U/HPLC, CE, SDS-PAGE, mass spectrometry, and other analytical technologies as applied to protein analytical method development, trouble shooting and validation for GMP release and stability testing.
$144,000 - $162,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Teleo is founded by Vinay Shet and Rom Clément, experienced technology executives who led the development of Lyft’s Self Driving Car and Google Street View. Teleo is backed by YCombinator, Up Partners, F-Prime Capital, and a host of industry luminaries.
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Out client is looking for a highly skilled, motivated, and creative analytical scientist to join their Vaccine Product Development organization as Scientist I within Protein Development and Clinical Manufacturing.
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Contribute to the development and implementation of case management programs and initiatives. Certified Case Manager (CCM), Certified Alcohol and Drug Counselor (CADC), or Mental Health First Aid.
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Candidates with B.S./M.S. may also be considered with demonstrated leadership track record in analytical development and drug product process development. ● Define analytical testing strategies of raw materials, biological starting materials, in-process samples, impurity quantitation, and drug product release and stability, including selection and development of fit-for-purpose methods.
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Broad hands-on experience with modern analytical instrumentations commonly used in the analysis and characterization of biologics, carbohydrates, conjugates and small molecule drug candidates and successful track record of method development trouble shooting and validation, e.g., UV-Vis, various modes of HPLC, CE, SDS-PAGE, icIEF, LCMS, GCMS, enzyme kinetics, colorimetric and fluorescent plate-based assays, ELISA, Western Blot, etc.
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Associate Director, Analytical Development, Raw Materials. Vaxcyte is looking for an energetic and talented individual to join our analytical development team. Independently perform method development across a broad range of analytical methods for raw materials for QC and characterization purpose to support pre-clinical and clinical projects.
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Novity has an immediate opening for a Predictive Maintenance Algorithm Development Engineer with a background in chemical process modeling, or modeling in related process industries, such as oil and gas, food and beverage, wastewater, or similar.
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Responsibilities include: Coordinating with the PCDI and AI Co-Chairs to support the research, development, and delivery of a broad portfolio of knowledge services for the practice. Office : Knowledge Management Attorney Title : Knowledge Management Attorney Location : Palo Alto Job Summary Gibson Dunn is a leading global law firm, advising clients on significant transactions and disputes.
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Actively participate in and lead new product development teams as it relates to supplier quality to support product and process design and development activities via leading the supplier risk management process.
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product development management drug jobs Title: development director in Redwood City, CA
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