Sr. Regulatory Affairs Specialist - Minneapolis

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

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 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 ...

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 ...

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 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. · ...

This role is responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process and sustaining engineering projects ensuring compliance with FDA and EU regulations ISO standards and other regulatory agencies. · ...

Senior Regulatory Affairs Specialist in Minneapolis. · ...

Job summaryDrive strategic influence by shaping policies, advocating for organizational goals, and navigating regulatory landscapes to create meaningful public sector impact. · ...

At Jack Link's, we feed the journey. · Create and assure compliance of federally regulated product label information. · ...

We are seeking a detail-oriented Regulatory Affairs Specialist to support compliance quality management and regulatory activities within the sterile processing medical device division This role ensures adherence to international regulations standards supports product registration ...

Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. · ...

The Advanced Regulatory Affairs Specialist will assist in regulatory submission, annual reports, registrations and listings while ensuring compliance with applicable medical device regulations. · ...

We are looking for a Sr. Regulatory Affairs Specialist to join our team at Jack Link's. As a key member of our regulatory affairs team, you will be responsible for creating and assuring compliance of federally regulated product label information. You will work cross-functionally ...

Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. · Regulatory Submissions: Author and compile CMC sections of regulatory applications. · Draft and maintain hig ...

Join Bio-Techne to enable cutting-edge research in Life Sciences and Clinical Diagnostics. We offer competitive insurance benefits starting on day one: medical, dental, vision, life, · short-term disability, · long-term disability, · pet, · and legal and ID shield.We invest in ou ...

Drive meaningful change by bridging our organization with governmental bodies. · Craft strategies · Advocate goals · ...

The job involves regulatory affairs activities such as submission to regulatory bodies and annual reports, while ensuring compliance with applicable medical device regulations. · Maintain regulatory files. · Coordinates with product development teams to request/report data for su ...

Responsible for regulatory affairs activities to assist in regulatory submission, annual reports, registrations and listings. · Works in the regulatory affairs department on assigned projects. · Maintain regulatory files. · ...

The Senior Regulatory Affairs Specialist will be responsible for developing and maintaining quality standards and protocols for processing materials into partially finished or finished products. · Data driven problem solving · Solid understand and application of regulatory requir ...