Senior Regulatory Affairs Specialist - Saint Paul

Regulatory Affairs Specialist is responsible for ensuring compliance with regulatory requirements and supporting product registrations. The role involves preparing and submitting regulatory documentation, maintaining databases and document repositories, and providing guidance to ...

Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. · B.A. or B.S. degree in life science field (biology, microbiology, ...

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 ...

Drive meaningful change by bridging our organization with governmental bodies. · Craft strategies, advocate goals, and navigate regulatory complexities with insight and passion for public policy. · ...

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

+Job summary · Join Thermo Fisher Scientific as a Regulatory Affairs Specialist III and contribute to ensuring compliance with global regulations while enabling our mission to make the world healthier, cleaner, and safer. · +Bachelor's degree or higher in a science or engineering ...

We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, · Join Thermo Fisher Scientific as a Regulatory Affairs Specialist III and con ...

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

We're hiring a Senior Regulatory Affairs Specialist to support global medical device compliance across the U.S., Canada, and Europe. · Maintain and update European technical documentation, · Prepare and manage annual regulatory registrations for the U.S. (FDA), Canada, and other ...

This position supports Medline's Northfield location and will travel up to 10% of the time. Under limited supervision the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects. They prepare comprehensive regulatory ...

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 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 ...

The Principal Regulatory Affairs Specialist is responsible for developing and implementing regulatory strategies across projects.This individual partners with internal stakeholders and external consultants to optimize and execute these strategies in support of business objectives ...

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 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 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 ...

Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. · In support of business priorities, determine the requirements for ...

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 ...

The Regulatory Affairs Specialist is responsible for ensuring materials, components, and finished products comply with global regulatory standards · Ensure company is compliant with global material and substance regulations, including EU REACH (SVHC, Annex XVII), EU RoHS, · Confl ...

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. · ...