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A scientific degree with directly relevant professional experience in small molecule development, global CMC regulatory affairs and CMC technical areas of at least 16 years with a BA/BS or 14 years with an MA/MS, PhD, PharmD, or MD.
$295,290 - $382,140ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Sr. Regulatory Affairs Specialist-CT/AMI. Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team members, cross-functional teams, and stakeholders.
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You've acquired a minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software (SiMD/SaMD) environments, including leadership/guidance on global regulatory strategy for 510K's, CE Marking per MDD, EU MDR (updating Technical Files), Worldwide product registrations, Design Dossiers, PMA, clinical evaluations, Post Market Surveillance and reviewing Marketing Communication materials for promotional purposes.
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Block is looking for an experienced policy and regulatory strategist to serve as our Head of Regulatory Affairs. Maintain fluency on a variety of regulatory and policy issues at the intersection of financial and technology policy, including financial regulation, consumer protection, tax, cryptocurrencies, AI/machine learning, intellectual property, and privacy.
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10+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs / small molecules.
$100 - $113 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Executive Office support: serves as Chief of Staff to the VP, Head of Alexion Regulatory Affairs, supporting internal and external engagement and managing activities as part of the function's Executive Office.
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Piper Companies is currently seeking a Regulatory Affairs Specialist, Cell & Gene Therapy for an opportunity in Philadelphia, Pennsylvania (PA), to join an innovative biotechnology company creating life-saving cell therapies.
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The Regulatory Affairs team monitors activity and advocates before state and federal economic regulators, transmission service providers and regional trade associations in the interest of Invenergy s operating and development assets.
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The Principal Scientist provides regional scientific and regulatory expertise and leverages scientific networks to enable the development and execution of Mars Wrigley (MW) Scientific and Regulatory Affairs (SRA) strategy.
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Within Global Regulatory Affairs, our Chemistry, Manufacturing and Controls (CMC) organization provides regulatory leadership to CMC development teams and the Pharma Supply Chain organization to enable approval of new medicines and uninterrupted supply of our medicines to patients.
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This executive will work internally and externally, maintaining and establishing critical relationships to fuel and amplify priorities in Washington, D.C. Serving as the manager of the Legislative Affairs and Regulatory teams, this Executive will closely coordinate with the Public Policy, External Affairs, Political and State and Local Government Affairs leadership in Washington, Philadelphia, and across the Comcast footprint.
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Job DetailsThe Director of Risk Management and Regulatory Affairs (Patient Safety Officer/Privacy Officer) serves as an accessible resource to the hospital and community on risk management and regulatory issues.
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Minimum 8-10 years of combined regulatory affairs experience in color cosmetics, both in domestic and international markets. Strong knowledge and expertise in international regulatory affairs and packaging/labeling compliance.
$130,000 - $150,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Typical Minimum Experience 13+ years of relevant Quality Assurance and Regulatory Affairs experience 5+ years of management experience 4-year degree in business or related field or equivalent experience Advanced degree a plus (MBA, MS) Must be able to travel up to 30-40% Critical Skills 5 + years’ experience working within Quality Assurance in a government regulated environment Accreditation experience with ISO Standards or regulatory agencies (DEA, FDA, etc.
$142,200 - $237,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Cross-functional clinical processes, including data management, biostatistics, medical writing, drug safety/pharmacovigilance, and regulatory affairs. Negotiates cross-functionally, successfully motivates and influences (Clinical Development, Regulatory Affairs, CMC, QA, Pharmacovigilance, etc.
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regulatory affairs jobs Title: regulatory specialist Company: Abbott Laboratories
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