The International Regulatory Affairs Specialist provides regulatory support for implantable neurostimulation therapy for the treatment of obstructive sleep apnea. Interact with international regulator...

Additionally, this individual is responsible for representing Regulatory Aff Regulatory, Regulatory Affairs, Global, Principal, Quality, Specialist, Manufacturing, Business Services. This Regulatory p...

Abbott is seeking a passionate, experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, MN. Acts as a regulatory representative on core product development teams, commun...

Complete FDA MDR and other outside competent authority regulatory reports.

Complete FDA MDR and other outside competent authority regulatory reports.

Abbott is seeking a passionate, experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, MN. Acts as a regulatory representative on core product development teams, commun...

Com Regulatory, Specialist, Remote, Health, Manufacturing, Healthcare. Responsible for coordinating the planning, preparation, assembly, review and publication of regulatory submissions to the FDA and...

Complete FDA MDR and other outside competent authority regulatory reports.

Complete FDA MDR and other outside competent authority regulatory reports.

Team with business unit Regulatory Affairs Specialists (RAS) and international regulatory staffs to provide regulatory support for changes to existing products. Work with RAS, engineers and technical ...

Team with business unit Regulatory Affairs Specialists (RAS) and international regulatory staffs to provide regulatory support for changes to existing products. Work with RAS, engineers and technical ...

Collaborate with Operating Unit Regulatory Affairs Specialists and international regulatory colleagues to provide regulatory support for new products/therapies and changes to existing products. Work w...

Team with operating unit Regulatory Affairs Specialists and international regulatory staff to develop and execute regulatory strategies for new and existing products, ensuring alignment with business ...

In alignment with responsible Regulatory Affairs Management, the Senior Regulatory Affairs Specialist, (Advertising/Promotion) is responsible for reviewing, editing and supporting compliance of SWMI a...

Document, code, and analyze complaints to identify trends and maintain compliance with regulatory standards. Regulatory, clinical, medical, or QA experience is advantageous. Familiarity with regulator...

This Regulatory professional will act as the primary Regulatory Affairs representative in projects and initiatives related to the Capital Equipment and Medical Electrical Equipment spaces. Actively pa...

Collaborate with the US Operating Unit Regulatory Affair team and international regulatory colleagues to provide regulatory support for new products/therapies or changes to existing products. Works wi...

Document, code, and analyze complaints to identify trends and maintain compliance with regulatory standards. Regulatory, clinical, medical, or QA experience is advantageous. Familiarity with regulator...

Abbott is seeking a passionate, experienced **Regulatory Affairs Specialist II** to join our team on-site in Plymouth, MN. In this role, you will perform specialized level work assignments and/or an...

Abbott is seeking a passionate, experienced **Regulatory Affairs Specialist II** to join our team on-site in Plymouth, MN. In this role, you will perform specialized level work assignments and/or an...

Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development team. Act...

This Regulatory Affairs Specialist II role will provide regulatory support on a wide variety of Interventional Cardiology devices with a focus on supporting US and EU compliance activities. Represent ...

We are recruiting for a **Regulatory Affairs Specialist III** to join our team on-site in Plymouth, MN. Provides support to Regulatory Affairs management when working towards resolution of complianc...

This Regulatory professional will act as the primary Regulatory Affairs representative in projects and initiatives related to the Supplier Quality, Material Controls spaces. Actively participate in va...

Actively participate in various Quality System Community of Practice forums as representative of Regulatory Affairs, assessing impact, and bringing awareness to Regulatory Teams across the divisions a...

Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development team. Pre...

Regulatory Affairs Operations Specialist I. Acts as a regulatory representative responsible for review and analysis of GTS blocked orders, providing guidance and direction on regulatory compliance. Th...

Remote-Medical Device Regulatory Affairs Specialist II. As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally...

Masters Degree in Regulatory Affairs preferred and may be used in lieu of direct regulatory experience. We are recruiting for a **Senior Regulatory Affairs Specialist** to join our team on-site in S...

QUALIFICATIONS OF THE REGULATORY AFFAIRS SPECIALIST:. REGULATORY AFFAIRS SPECIALIST OVERVIEW:. The Regulatory Affairs Specialist will focus on assisting with maintaining product compliance with FDA/MD...

Remote-Medical Device Regulatory Affairs Specialist II. As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally...

Remote-Medical Device Regulatory Affairs Specialist II. As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally...

The International Regulatory Affairs Specialist provides regulatory support for implantable neurostimulation therapy for the treatment of obstructive sleep apnea. Interact with international regulator...

Maintain Regulatory Affairs product files to support compliance. Author and prepare regulatory submissions for new products and changes. Review significant regulatory issues with supervisors and resol...

The Regulatory Affairs Specialist II will support the IA business unit in meeting global registration requirements. As a regulatory process expert supporting global registrations the candidate interpr...

The Specialist II is responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development process, integration of acquired products, and ongoing regulatory compl...

The Specialist II is responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development process, integration of acquired products, and ongoing regulatory compl...

Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awareness to Regulatory Teams. Perform as the Regul...

Have a passion for regulatory affairs? Interested in medical software? Look no further! We are looking for a savvy and passionate Senior Regulatory Affairs Specialist to join our team here at Canon Me...

The Regulatory Affairs Specialist will develop strategies and submissions for projects and issues related to regulatory documents, global submissions, investigations, product development planning, and...