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The Regulatory Specialist will be responsible for a wide range of duties related to regulatory compliance, data analysis, stakeholder collaboration, system management, and program implementation in the healthcare setting.
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The Associate Specialist SRA supports the function in the areas of global raw material compliance, regulatory data management and digital transformation to unlock value and efficiency. Executes precise and accurate data entry/data management of high-risk regulatory information in Mars's suite of product lifecycle systems- regulatory information includes nutrition, ingredient composition, claims suitability, lifestyle suitability, food additive compliance, allergen labelling.
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Piper Companies (Health & Sciences) is seeking motivated candidates for a Specialist, Regulatory Affairs opportunity in the Rockville, MD Area for immediate assistance with an established research firm supporting critical research trials.
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TA specialist collaborates with affiliate MI and relevant internal partners who may include medical affairs, development, regulatory, global patient safety and operations, and commercial, to manage global response topics and content.
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Regulatory Affairs Specialist. regulatory experience (SEC, FINRA, CBOE, NFA, CFTC, etc.) The Firm's Regulatory Group is housed within its Legal Department. This hire will be a member of the Firm's Regulatory group which is responsible for exam oversight, branch inspections, regulatory change tracking, governance related tasks and additional ad-hoc tasks.
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BA/BS degree in a technical or scientific discipline such as biology, chemistry, physiology, engineering, medical or law or related regulatory affairs experience with medical devices or pharmaceuticals.
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Regulatory Affairs Specialists will be directly involved in ensuring regulatory compliance and administrative management for multiple clinical trials, working closely with investigators, industry sponsors, contract research organization representatives, and UAMS institutional oversight offices.
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Project Specialist I, Rates and Regulatory Affairs. Maintain alignment of regulatory compliance strategies to all key local functional areas. Liaises with regulatory authorities and commission staff and may participate in industry forums to promote regulatory compliance.
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Provide assistance to business development at client presentations, bid defense meetings, and the like in various regulatory aspects (at the discretion of Senior Regulatory Affairs staff.
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The Regulatory Specialist II is an intermediate level position supporting regulatory affairs in clinical trial research. Incumbents are responsible for coordinating and supporting regulatory affairs activities for non-interventional and interventional trials for IRB submission.
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Then come and join our global team as Regulatory Affairs Specialist to support international registrations. Acting as a Regulatory Affairs subject matter expert on new product introduction and design control teams.
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team members, cross-functional teams, and stakeholders. The Senior RA Specialist will play a critical role in ensuring Philips Computed Tomography (CT) and Advanced Molecular Imaging (AMI) solutions are safe, reliable, and compliant through driving global regulatory strategy and regulatory roadmaps-understanding competitive claim landscape, legislative initiatives, and marketing strategy.
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Senior Regulatory Affairs Specialist near Cuyahoga Falls, OH. Senior Regulatory Affairs Specialist. 5+ years of progressive experience in regulatory affairs required.
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Job Segment: Compliance, Law, Manager, Regulatory Affairs, Legal, Automotive, Management. Oversee and manage a regulatory specialist. The Senior Regulatory Compliance Manager is principally responsible for definition and management of Kia's CAFÉ and GHG compliance strategies, and formulating related recommended product actions (powertrain, volume/mix, distribution) necessary to comply.
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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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