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The (Temp) Regulatory Affairs Associate - EU MDR Technical Documentation reports to the Regulatory Affairs Director and will work with the Iridex Team (including both Regulatory and Cross-functional colleagues) and consultants to obtain, prepare, and provide information in support of EU MDR submission.
$35 - $45 an hourExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Executive Director/ Sr. Director of Medical Affairs. As a key member of Adicet's medical team, the head of Medical Affairs will be responsible for setting up and overseeing effective interactions with key opinion leaders, patient advocacy groups, and medical institutions in areas of hematology-oncology and autoimmune diseases relevant to Adicet's pipeline.
$297,000 - $409,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As the administrative leader for the department, the DFA provides leadership and direction for all financial and administrative functions, including budgeting and financial management, strategic planning, human resources, grant and contract administration, academic affairs, facilities/space planning, compliance, and safety.
$199,000 - $291,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We are looking for a Sr. QA Automation Engineer - Bixby who will be responsible for expertise in AI, large scale data analysis, statistical analysis, deep learning, computer vision, robotics and language understanding to join us.
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Array Labs is building a distributed radar imaging constellation to power the first accurate, real-time 3D model of the world.
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Partner with other teams involved in the end-to-end assay launch and maintenance processes, including Clinical Ops, Clinical Lab, Quality, Regulatory Affairs, Medical, Business Stakeholders, etc.
$90,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Sr. Component Engineer is responsible for consumable plastic component design and improvement. Use CAD modeling, prototyping, molding simulation CAE data, and hands-on lab testing to develop and enhance part attributes, mold concepts, and mold design details.
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This role is expected to closely collaborate with multiple teams across Process Development, MSAT, Analytical Development, Regulatory Affairs, Quality and Manufacturing. The Sr. Engineer/Scientist in Process Development, CMC will focus on commercialization and post-commercial process optimization of allogeneic cell therapy manufacturing processes.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Global regulatory affairs experience (FDA, MDD/CE/MDR, UKCA, etc.) Provide support and guidance for introducing and maintaining medical devices in global markets, which may include duties like documentation, auditing support, risk analysis, complaint investigation and handling, CAPA, regulatory submissions, post-market surveillance, and more.
$75,000 - $78,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This goes for the emissions-free Electric Adventure Vehicles we build, and the curious, courageous souls we seek to attract.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Adicet Bio is seeking an exceptionally talented and motivated individual to join our team as a regulatory associate I/II. This position will be responsible for supporting the Sr. manager of regulatory affairs and assisting in developing and executing regulatory activities in support of the CMC, nonclinical, and clinical development for our early development pipeline products within the Regulatory Affairs department.
$105,000 - $146,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Advise internal cross-functional team who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, & others such as Commercial.
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Solid understanding of manufacturing processes, quality systems, and regulatory requirements. Implement robust quality control measures to ensure product reliability, consistency, and compliance with regulatory standards.
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PAVIR engages in the administration of funds and providing support for the conduct of research at the Veterans Affairs Palo Alto Health Care System (VAPAHCS) to find new and improved ways to combat human disease and help people with disabilities.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Sr Director Manufacturing & Sustaining Engineering, Instruments will lead multiple leaders in the engineering organization of NPI Engineering, Sustaining Engineering, Service Engineering, Supplier Development Engineering, Technical Sustaining Engineering, and providing technical leadership and guidance to the entire Instrument Operations team.
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affairs job Title: sr regulatory affairs Company: Thermo Fisher Scientific in Los Altos, CA
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