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Senior Regulatory Affairs SpecialistWe're hiring a Senior Regulatory Affairs Specialist to support U.S. and global regulatory submissions for medical devices and partner with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.Key ResponsibilitiesPrepare and support submissions including IDEs, 510(k)s, CE Technic...
Regulatory Affairs Specialist ResponsibilitiesSupport development activities for medical device software products.Develop regulatory strategies and prepare submissions for markets including the United States, European Union, and Canada.Collaborate with regional regulatory teams to align global regulatory strategies.Review and approve product label...