Associate Regulatory Affairs Specialist - Hopkins

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 ...

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. · ...

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 ...

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 ...

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 ...

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 ...

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'd lik ...

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 ...

We are seeking a passionate and experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, MN. This role will lead the preparation and submission for regulatory approvals and identify and resolve problems. · ...

The primary purpose of this job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals within the United States and International markets. · We create better solutions · Collaboration · We create suc ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. · ...

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 ...

The primary purpose of this job is to provide team support to Regulatory Affairs managers and department management in being responsible for ensuring compliance to all relevant regulations and standards. · You adhere to Integer's Values and all safety, environmental, security and ...

This Sr. Regulatory Affairs Specialist I position is primarily remote but requires occasional onsite presence at the global headquarters and other sites as needed. · Market Access – Ensure market access of our products World-Wide · Support assessments and completion of documentat ...

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 ...

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 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. · ...

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 ...