Senior Regulatory Affairs Specialist - Maple Grove

Expected Travel · : Up to 10% · Requisition ID · : 13226 · About Teleflex Incorporated · As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in h ...

The Sr. Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies, assessments and submissions for complex projects across multiple business units and review issues related to regulatory documents. · ...

+ Serve as a regulatory affairs specialist supporting product corrections and recalls in collaboration with the Field Action Team. · + Coordinate communication with internal OUS regulatory partners and external regulatory authorities for recall-related activities. · + Manage Prod ...

The Sr. Regulatory Affairs Specialist will develop US EU and Canada strategies assessments and submissions for complex projects across multiple business units. · Conduct appropriate research using standards guidance documents previous assessments and other resources to develop st ...

Join our Vascular Therapies Regulatory Team where we develop innovative technologies to treat peripheral vascular disease. Our products improve patient outcomes and enhance lives by delivering some of the most advanced and comprehensive therapy solutions on the market. · ...

The Sr. Regulatory Affairs Specialist will develop US, EU, and Canada strategies, assessments and submissions for complex projects across multiple business units and review issues related to regulatory documents, investigations, product development planning and regulatory agency ...

The Sr. · Regulatory Affairs Specialist (SRA) will develop US, EU, · & Canada strategies, assessments and submissions for complex projects across multiple business units and review issues related to regulatory documents, · investigations, product development planning and regulat ...

Join our Vascular Therapies Regulatory Team, where we develop innovative technologies to treat peripheral vascular disease. Our products improve patient outcomes and enhance lives by delivering some of the most advanced and comprehensive therapy solutions on the market. · ...

We're hiring a Senior Regulatory Affairs Specialist to support innovative growth initiatives within our Cardiology division, · a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level.This high-impact role will drive regulator ...

Join our Interventional Cardiology and Vascular Therapies team, where we create innovative technologies to diagnose and treat peripheral vascular disease. Our products—including medical electrical equipment such as consoles, catheters, and other associated devices—improve patient ...

· We believe that great healthcare is an essential safeguard of human dignity.   · At Laborie, we know the work we do matters – it's what fuels our motivation and contributes to our success. If you're ready to make a positive impact in the lives of patients across the globe, we' ...

+We are looking for a passionate Regulatory Affairs Specialist who has experience supporting regulatory submissions for both the Americas and the EU. · +Providing expert advice on regulatory requirements · ...

Abbott is recruiting for a Regulatory Affairs Specialist III to join their team on-site in Plymouth, MN.This new team member will support manufacturing/operations day-to-day activities for change control and provide regulatory direction on team activities. · ...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all A Day in the Life REGULATORY AFFAIRS SPECIALIST · Onsite · The Regulatory Affairs Specialist develops strategies for worldwide product registrat ...

We anticipate the application window for this opening will close on - · 16 Feb 2026 · A Regulatory Affairs Specialist helps develop strategies for worldwide product registration with Medtronic Geography Regulatory partners and global regulatory agencies to introduce products and ...

We anticipate the application window for this opening will close on - 16 Mar 2026 · At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innova ...

We are looking for a passionate Regulatory Affairs Specialist who has direct experience submitting regulatory submissions for both the Americas and the EU. · Providing advice on regulatory requirements · Preparing submissions · Negotiating their approval · Assisting with license ...

All required qualifications must be documented on application materials. · Required Qualifications · Bachelor's degree + 6 years experience in clinical research or an advanced degree + 4 years experience in clinical research. · Demonstrated ability to lead and drive initiatives t ...

We anticipate the application window for this opening will close on February 16th,2026.At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. · ...

We are seeking a highly skilled Regulatory Affairs Specialist with 4–6 years of experience to join our team on a fast-paced engagement. · We are based in a hybrid work model in Minneapolis/Plymouth Minnesota and this role focuses on supporting urgent international product registr ...