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Senior Regulatory Affairs Specialist
San Francisco$120,000 USD a year

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
Los AngelesNegotiable

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...

Regulatory Specialist
BrusselsNegotiable

Regulatory Affairs Specialist - Medical Devices Location: Belgium (Hybrid)Industry: Medical Devices / Medical Equipment Manufacturing About the Role An established international medical device organisation is seeking a Regulatory Affairs Specialist to support regulatory market access, product lifecycle management, and compliance activities across ...