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About the role: The Medical Affairs Manager (MAM) role is responsible for executing the Medical Affairs strategy, specifically for the Peripheral Arterial portfolio to support device education and adoption specific to clinical use, clinical data, and clinical impact for Health Care Providers (HCPs.
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We are seeking a talented and motivated Regulatory Affairs Specialist to join our dynamic team in Plymouth, MN. This is a hybrid role, providing the flexibility to work both onsite and remotely, with the possibility of converting to a full-time position for the right candidate.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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Regulatory affairs certification (RAC) or relevant professional certification (e.g., ASQ Certified Quality Auditor) preferred but not required. Collaborate with cross-functional teams, including manufacturing, quality assurance, quality control, regulatory affairs, and supply chain, to address GMP-related issues and drive continuous improvement initiatives.
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The Regulatory Affairs Specialist (RAS) is responsible for collaborating, planning and executing regulatory activities related to modifications of the Lung Health product portfolio. Bachelor’s degree with 2+ years of medical device regulatory affairs experience.
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Support projects or other initiatives from cross-functional groups and departments (i.e., Project Management teams, Scientific group, Quality/Compliance, Data Management, Biostatistics and Regulatory Affairs), and ensure adequate safety support and timely update of safety information to internal and external stakeholders.
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Communicate and collaborate effectively with Sales and Marketing, R&D, Regulatory Affairs, Quality Engineering, and Medical Affairs in completing clinical evaluation project-related deliverables.
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JOB DESCRIPTION Job TitleSr. Manager- Regulatory AffairsJob DescriptionThe Senior Manager Regulatory Affairs will play a critical role within Philips’ Clinical Informatics organization by leading regulatory projects for Philips’ Disease Management Solution products, ensuring and maintaining global accurate regulatory strategy and market access, directly impacting the lives of patients around the world.
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Regulatory Affairs Specialist III. Job Family Group: Regulatory Affairs Career Band Level: P3. TGA and China CDA; or 2 years of experience with Master’s in Regulatory Affairs. Integer Holdings Corporation (ITGR) is one of the largest medical device outsource (MDO) manufacturers in the world serving the cardiac, neuromodulation, orthopedics.
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GPAC (Growing People and Companies) is an award-winning search firm specializing in placing quality professionals within multiple industries across the United States since 1990. Responsibilities: Install, maintain, and repair fire alarm systems, electronic security systems, and CCTV systems.
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Accountable and Reports to: District Store Director, Store Manager, Assistant Manager of; Store Operations, Perishables, and Health Wellness Home; Food Service Director; Coffee Shop Department Manager.
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The role requires close collaboration with R&D, marketing, sales, regulatory, Medical/Clinical/Scientific Affairs, Legal and other cross-functional teams to ensure the products meet customer needs and regulatory requirements while driving business growth.
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The Medical Support Specialist follows guidance provided by BioLife Medical Affairs and provides center level support of environmental, health and safety (EHS). You can be a Pandemic Coordinator when authorized by EHS and support investigations associated with pandemic threats within the local community as indicated by EHS or Medical Affairs.
$35.96 an hourFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Job Title: MDR - Principal Regulatory Affairs Specialist. Job Title: MDR - Principal Regulatory Affairs Specialist. Drafting 510(k)s to be submitted to FDA regarding changes driven by MDR. EU MDR Technical Documentation completion in addition to supporting responding to Notified Body questions (Working with a cross functional team.
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Five to ten years’ experience in a senior level leadership role (General Manager or Senior Manager) in a theater, retail or hospitality environment. The Operations Manager provides support to the Director of Operations to ensure all management teams are operating in accordance with policies, goals, and objectives and contributing to enhancing the overall Emagine guest experience.
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affairs job Title: affairs manager Company: Gpac in Osseo, MN
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