Regulatory Specialist Jobs
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Regualtory Affairs Specialist
Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...
Senior Regulatory Affairs Specialist
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...
Regualtory Affairs Specialist
Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...
Regulatory Specialist
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 ...
Senior Regulatory Affairs Specialist
Senior Regulatory Affairs Specialist Overview Join a growing neurovascular medical device team supporting regulatory compliance and product lifecycle activities for innovative technologies used to treat stroke and other neurovascular conditions. This onsite position (4 days/week) partners closely with engineering, quality, clinical, and commercial ...
Regulatory Affairs Specialist
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...
