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Lead the organization’s ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Reporting to the COO, The Vice President, GxP Quality Assurance is responsible for establishing and leading Aveo’s Quality Management System (QMS) operations and ensuring compliance with Local, State, Federal, and International regulations and standards associated with GXPs and Quality Systems in a fast-paced, primarily virtual development environment.
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Understand and follow SOPs, safety procedures, and quality assurance guidelines for animal care at all levels of biohazard containment (BSLI and BSLII). Innovive, a high-growth manufacturing company serving the Biomedical Research community is looking for Animal Care Technicians.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Job Overview: The Executive Director, Quality Assurance, GMP will oversee internal and external GMP quality and leverage extensive quality and manufacturing experience from all clinical phases into commercialization.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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We are seeking a highly organized and experienced Quality Assurance (QA) Manager with strong people management skills to lead our Boston team and ensure overall GxP compliance. Not less than six (6) years' experience in GLP/GCLP quality assurance (QA.
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The ideal candidate will have experience in the biotech or medical device industry and a strong background in process engineering, quality assurance, and production optimization. As a Manufacturing Engineer on the team, you will posses a passion for optimizing manufacturing processes, ensuring product quality, and driving continuous improvement.
$50 - $55ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This could be a manager or quality engineering manager level role, with the ability to own the continuous improvement and quality assurance processes globally. Senior Quality Engineer/Manager position.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Supplier Quality Management:Develop and manage supplier quality assurance programs. Experience:Minimum of 10 years of experience in quality assurance or quality control.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Lead quality assurance for CMO-related activities, overseeing GMP compliance for manufacturing, testing, and release processes along with batch reviews and tech transfers. Bachelors in life sciences with 12+ years in GMP quality leadership, expertise bringing pharmaceutical products through clinical stage into production, and experience in external manufacturing model are required.
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This includes continuous communication with Quality Assurance, Quality Control, Upstream and Downstream Process Development, Drug Product Development, Analytical Sciences and Supply Chain teams to ensure efficient tech transfer of Alexion's clinical drug substance manufacturing activities.
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Effectively manage project risks, specifically those intrinsic to the offshore wind industry, manufacturing, Quality Assurance/Quality Control, and supply chain challenges.
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Additionally, the Associate Director, Lab Operations Service Management, Business Engagement & Technology will ensure team members maintain reliable, scalable and compliant systems that easily meet business needs by efficient delivery of support services that ensures uninterrupted lab research, quality control and manufacturing shop floor operations.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Director GMP Quality Assurance will collaborate with the CMC department and external Vendors to ensure oversight and compliance. Sr Mgr/Associate Director, GMP Quality Assurance.
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Must demonstrate knowledge of several allied fields, such as chemical engineering, analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs.
$266,200 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Will provide QA oversight of the quality control bioassay and flow cytometry laboratories along with raw material, analytical development, and supply chain groups in support of Vertex Clinical Cell and Gene Therapy Programs.
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manufacturing quality assurance jobs in Boston, ID, France
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