Sr Regulatory Affairs Specialist I - Eden Prairie, MN

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Gu ...

Solventum enables better healthcare by pioneering game-changing innovations at the intersection of health, material science that change patients' lives. · ...

At Solventum we enable better smarter safer healthcare to improve lives.We pioneer game changing innovations at the intersection of health material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. · Deve ...

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. · Developing and executing regulatory strategies to achieve new product market authorizations faster than competitors and ...

We enable better, smarter, safer healthcare to improve lives.As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change pa ...

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Gu ...

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. · Developing and executing regulatory strategies to achieve new product market authorizations faster than competitors · M ...

Overview · Diagnostic Group, LLC is part of the Demant Group. Demant is a world-leading hearing healthcare group that for more than a century has played a vital part in developing innovative technologies and know-how to help improve people's hearing and health. In every aspect, f ...

Diagnostic Group LLC is looking for an experienced Regulatory Affairs Specialist-Product Development to ensure products comply with all applicable regulatory requirements including FDA EU MDR and ISO This role supports product development and serves as a key resource for regulato ...

We are hiring an Associate Regulatory Affairs Specialist to work within either our Hopkins, MN or Marshall, MN offices. The right candidate is responsible for leading regulatory affairs projects and teams as assigned. · The incumbent works under the guidance of project leaders to ...

We are hiring an Associate Regulatory Affairs Specialist to work within either our Hopkins, MN or Marshall, MN offices. · The right candidate is responsible for leading regulatory affairs projects and teams as assigned.Generate and approve food label information including ingredi ...

This role involves preparing regulatory submissions for new products changes renewals to support global market access collaborating with cross-functional teams ensuring product documentation aligns with applicable regulatory requirements. · ...

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

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 ...

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 ...

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. · ...

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 experience supporting regulatory submissions for both the Americas and the EU. · +Providing expert advice on regulatory requirements · ...