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Principal Regulatory Affairs Opportunity - Global Semaglutide PortfolioWe are supporting a leading global pharmaceutical company in the search for a Principal Regulatory Affairs professional to join a high-profile regulatory team responsible for post-marketing activities across a market-leading chronic disease portfolio.This position offers the opp...
An innovative commercial-stage biotechnology company is seeking a Senior Regulatory Affairs Specialist to support regulatory compliance and submission activities across both marketed products and development-stage programs. This individual will contribute to regulatory strategy, health authority interactions, and global submission activities while ...
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 ...
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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...