Regulatory Affairs Specialist: Average Salary in Minnesota in 2025

A company is looking for a Senior Regulatory Affairs Specialist - IVD. ...

REGULATORY AFFAIRS SPECIALIST OVERVIEW:. The Regulatory Affairs Specialist will focus on assisting with maintaining product compliance with FDA/MDSAP, ISO, and MDD/MDR requirements. DUTIES AND RESPONSIBILITIES OF THE REGULATORY AFFAIRS SPECIALIST:. QUALIFICATIONS OF THE REGULATORY AFFAIRS SPECIALIST...

Job TitleAerospace and Defense Regulatory Affairs Specialist. As a Aerospace and Defense Regulatory Affairs Specialist you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Leads… ensures products, systems, or processes mee...

They're looking for an experienced regulatory affairs professional who can independently manage post-market submissions assess changes, and collaborate across teams. Master's in Regulatory Affairs is a plus. Regulatory assessments after market changes. ...

Minimum of 5 years of experience in Regulatory Affairs and/or Quality, with at least 2 years' experience working in Regulatory Affairs, preferably in the medical device industry. We are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist to join our Peripheral Interventi...

As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environment. Principal Regulatory Affairs Specialist. This position performs specialized level work assignm...

As a Regulatory Affairs Specialist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Determining regulatory pathway through a global regulatory assessment of product changes including developing and maintaining documen...

As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environment. Principal Regulatory Affairs Specialist. This position performs specialized level work assignm...

As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environment. Principal Regulatory Affairs Specialist. This position performs specialized level work assignm...

Global Respiratory Protection Regulatory Affairs and Standards Development Specialist, Personal Safety Division. In this role as Global Respiratory Protection Regulatory Affairs Specialist you will play a key role in advancing occupational health and safety (OHS) culture and practice across 3M’s glo...

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 resolve submission issues. Develop regulatory strategies and provide ongoing support to project teams. ...

The International Regulatory Affairs Specialist provides regulatory support for implantable neurostimulation therapy for the treatment of obstructive sleep apnea. Interact with international regulatory partners in local offices to support submission contents, as well as foreign regulatory agency rev...

Global Respiratory Protection Regulatory Affairs and Standards Development Specialist, Personal Safety Division. In this role as Global Respiratory Protection Regulatory Affairs Specialist you will play a key role in advancing occupational health and safety (OHS) culture and practice across 3M’s glo...

Senior Regulatory Affairs Specialist. Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development team. Certific...

REGULATORY AFFAIRS SPECIALIST OVERVIEW:. The Regulatory Affairs Specialist will focus on assisting with maintaining product compliance with FDA/MDSAP, ISO, and MDD/MDR requirements. DUTIES AND RESPONSIBILITIES OF THE REGULATORY AFFAIRS SPECIALIST:. QUALIFICATIONS OF THE REGULATORY AFFAIRS SPECIALIST...

Regulatory Affairs Specialist is responsible for creating and assuring compliance of federally regulated product label information, including nutrition, ingredient declaration, allergens, claims and associated product communication. Contribute to the advancement of the Regulatory Affairs team, ident...

The Principal Regulatory Affairs Specialist is responsible for developing and implementing regulatory strategies across projects, processes, and/or products. This role provides hands-on regulatory affairs support for new product marketing submissions and changes to existing devices, including develo...

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 interprets federal/state/international regulations as they apply to our products, processes, and procedures...

Regulatory Affairs Specialist is responsible for creating and assuring compliance of federally regulated product label information, including nutrition, ingredient declaration, allergens, claims and associated product communication. Contribute to the advancement of the Regulatory Affairs team, ident...

As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environment. Principal Regulatory Affairs Specialist. This position performs specialized level work assignm...

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 Medical! As the Senior Regulatory Affairs Strategist, you will champion U. Support legal/regulatory ac...

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. In this role, you will lead the preparation and submission for regulatory approvals and identify and re...

Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awareness to Regulatory Teams. The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory prod...

Minimum of 5 years of experience in Regulatory Affairs and/or Quality, with at least 2 years' experience working in Regulatory Affairs, preferably in the medical device industry. We are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist to join our Peripheral Interventi...

The Senior Medical Safety Specialist works with minimal supervision on a range of medical safety activities of varying complexity in collaboration with Medical Safety team members and other functions, including Regulatory, Quality/Post-Market vigilance, Risk Management, Complaint Handling, Product D...