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The Principal Regulatory Affairs Specialist- SW & AI will shape, lead and execute innovative regulatory strategies to drive innovation within the Philips Innovation and Strategy organization globally.
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The Principal Regulatory Affairs Operations Specialist will report to the Regulatory Affairs (RA) Operations Manager and be responsible for assuming the regulatory functional owner role of the Philips data management solution (Rimsys), providing testing support for upgrades and releases of Philips tools, tracking and reporting global regulatory submissions and licensing data, and identifying and resolving issues related to regulatory master data.
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The Principal Regulatory Affairs Specialist will play a critical role in ensuring our Coronary Vascular products are safe, reliable, and compliant with global regulatory standards through team leadership and providing regulatory guidance for Sustaining and New Product Development/Design initiatives for our Image Guided Therapy Devices/Coronary Vascular team.
$97,000 - $178,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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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. Job Title Sr. Regulatory Specialist-CT/AMI Job Description 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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The Senior Regulatory Affairs Specialist is responsible for regulatory compliance, strategy and submissions related to accessory devices/products (mixture of class 1 and class 2.
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Senior Regulatory Affairs Specialist (U.S. Hub based location) The Senior Regulatory Affairs Specialist will leverage their industry knowledge to guide regulatory strategies efficiently.
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Job Title Senior Regulatory Affairs Specialist Job Description. You have a bachelor’s degree or equivalent internationally acquired qualification preferably in Regulatory Affairs and/or a science related field or equivalent experience in the medical device industry.
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Senior Regulatory Affairs Specialist. Mentor other regulatory affairs personnel within the team. Analyze and optimize RA processes together with cross-functional partners such as Quality Management, Regulatory Affairs, Clinical Affairs, etc.
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The Principal Regulatory Affairs Specialist is responsible for regulatory compliance, strategy and submissions related to accessory devices/products (mixture of class 1 and class 2.
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Principal Regulatory Affairs Operations Specialist (Colorado Springs/Plymouth/San Diego) Principal Regulatory Affairs Operations Specialist. Track and report global regulatory submissions and licensing data for Regulatory Affairs marketing authorizations, by maintaining internal Regulatory Affairs submission dashboards and trackers based on country approvals and registrations.
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The Principal Regulatory Affairs Specialist will prepare comprehensive regulatory strategies for complex new devices and post market changes within our Ultrasound business.
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Principal Regulatory Affairs Specialist (U.S. Hub based) Lead and enable strong cross-functional partnership between Regulatory Affairs and all key stakeholders including R&D, Marketing, Quality, Clinical Affairs and other functions at all levels within the business, and the local RA teams in the Philips international markets organization.
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Principal Regulatory Affairs Specialist- Software & Artificial Intelligence (U.S. Hub Based) Principal Regulatory Affairs Specialist-Coronary Vascular. Job Title Principal Regulatory Affairs Specialist Job Description.
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Principal Regulatory Affairs Specialist. Lead project teams for end-to-end Regulatory Affairs input and deliverables for new product introductions and product changes across the globe.
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