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Experience with preclinical and clinical regulatory affairs topics. Just-Evotec Biologics is seeking a Senior Director of Regulatory CMC to join a fast-paced, collaborative and multi-disciplinary team to lead all aspects of regulatory affairs for the advancement of low-cost biotherapeutics manufacturing.
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Partner with a variety of Microsoft subject-matter experts (SMEs), including Commerce/Payments & FinTech, Privacy & Regulatory Affairs, Intellectual Property Group, Competition, Office of Critical Infrastructure, Office of Responsible AI, Digital Safety, Environmental Sustainability, and others, to track and interpret regulatory requirements and developments worldwide.
$248,800 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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2 years of experience as a Regulatory Affairs Specialist, Clinical Data Analyst, or similar regulatory compliance role. Bachelor’s degree in Healthcare Administration, Pharmacy Administration, Regulatory Affairs, or similar healthcare field.
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As part of a small, passionate, and accomplished team of experts in the Legal and Compliance Department, you will help shape the company s regulatory affairs program. Beyond providing counsel as a subject matter expert in the areas described below, you will develop processes and tools to amplify the impact of the program and ensure the timely and efficient delivery of regulatory legal support.
$194,040 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Head of FDA Regulatory Affairs will play a leading role in assembling regulatory submissions to the FDA and overseas governmental agencies. Unusually for a modern biotech, Lumen is vertically integrated: everything from hit-to-lead discovery through GMP manufacturing and regulatory affairs is operated directly out of its Seattle campus.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Serve as liaison for internal regulatory bodies (IRB, Clinical Research Support, Regulatory Affairs, etc. A minimum of 3 years relevant experience in oncology quality assurance, regulatory affairs, or clinical research/study coordination function required.
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Experience in hazardous materials compliance, operations, or regulatory affairs, system configurations, auditing, project planning, and implementation is preferred. We are looking for a Compliance Systems Policy and Audit Manager to join the Regulatory Compliance team within the Dangerous Goods and Storage Compliance program, based in our headquarters in Seattle, WA. This role supports the integration of worldwide hazardous materials (hazmat) regulations into Amazon's regulatory modeling and technical systems.
$142,800 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Regulatory Affairs Manager - Permanent - Seattle, WA. Proclinical is seeking a Manager, Regulatory Affairs for a global medical device company. Responsible for developing and implementing global regulatory strategy and roadmaps through deep understanding of the competitive market landscape, regulatory / legislative initiatives, and product marketing strategy for product portfolio.
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5+ years experience in medical device quality and/or regulatory affairs. Responsible for executing and managing the Global Audit program, including medical device regulatory body inspections and internal audit program.
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Biomanufacturing courses: Quality control/quality assurance, introduction to bioreactors & cleanroom dynamics, regulatory affairs, introduction to aseptic technique. Biotechnology program courses: Protein purification using AKTA, flow cytometry, bioinformatics, independent research, cell culture (mammalian, insect.
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You will be an individual contributor reporting to the Director of Regulatory Affairs & Ethics. We're looking for a passionate Director of Legal to join our dynamic and collaborative Global Policy and Regulatory Affairs team at Atlassian.
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The successful candidate will see T-Mobile’s “big picture,” think strategically, advance our corporate and government affairs narrative, manage interactions across multiple teams in different locations, focus on priorities and push back when needed.
$160,400 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In partnership with Clinical Research, Medical Affairs and Development functions, ensures that all clinical trial activities are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global registration and commercialization of Gilead’s products.
$185,350ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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4+ years of relevant experience in safety, compliance, and/or regulatory affairs, including experience developing and implementing safety strategies and programs examples: OSHA and regulations, policies, and guidance.
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Since being founded the team has seen phenomenal and sustained organic growth, working across Medical Affairs, Publications, Promotional, Commercial and Regulatory spaces for their roster of blue-chip pharmaceutical companies and biotech's.
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regulatory affairs jobs in Bellevue, WA
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