Ethics and Regulatory Specialist - Saint Paul, MN

The Regulatory Licensing Specialist is responsible to determine, prepare, and submit required licensing in adherence with industry standards and protocols across the United States and Canada. · Determine licensing and regulatory submissions required and prepare documentation for ...

+The Regulatory Licensing Specialist is responsible to determine, prepare, and submit required licensing in adherence with industry standards and protocols across the United States and Canada. · +Determine licensing and regulatory submissions required and prepare documentation fo ...

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 ...

The Senior Regulatory Licensing Specialist is responsible for managing a diverse portfolio of wholesale distributor and pharmaceutical licenses across the United States and Canada. This role handles complex licensing issues, conducts regulatory research, and ensures timely licens ...

The Senior Regulatory Licensing Specialist is responsible for managing a diverse portfolio of wholesale distributor and pharmaceutical licenses across the United States and Canada. · This role handles complex licensing issues, conducts regulatory research, and ensures timely lice ...

Job Summary · 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. Prepare comprehensive regulatory strategies for new de ...

The Senior Regulatory Licensing Specialist is responsible for managing a diverse portfolio of wholesale distributor and pharmaceutical licenses across the United States and Canada. · Oversee a portfolio of licenses for wholesale distributors, third-party logistics providers, 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. · 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 ...

The Epilepsy Institute in the Department of Neurology is hiring a Regulatory Specialist (Research Professional 2) for an interdisciplinary array of clinical research studies ranging from pre-clinical animal and lab studies, pharmacological treatments, and/or medical devices. · Pe ...

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 ...

+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 ...

Work Schedule · Standard Office Hours (40/wk) · Environmental Conditions · Office · Job Description · As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life ...

Regulatory Specialist job description · Darcy Solutions is seeking a highly motivated and entrepreneurial Regulatory Specialist to join our growing company and help shape our future. This person will help drive regulatory compliance, facilitate expansion into new regions, and ens ...

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 ...

We're hiring a Senior Regulatory Affairs Specialist to support global medical device compliance across the U.S., Canada, and Europe.This role is ideal for a hands-on regulatory professional who has worked in an FDA-regulated, ISO-certified environment. · Maintain and update Europ ...

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 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 ...

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 ...