Regulatory Affairs Specialist
MED Medtronic Inc
Medtronic is seeking a Regulatory Affairs Specialist based in Mounds View, MN. This role focuses on worldwide product registrations for diagnostic devices, pacemakers, ICDs, CRT devices, and related software, with a strong emphasis on regulatory strategy and cross-functional collaboration. The position requires at least 2 years of medical device regulatory experience, knowledge of FDA guidelines, ISO standards, and the ability to communicate with regulatory authorities. #J-18808-Ljbffr
$107.2k - $160.8k
...font-size: 30px; font-weight: bold; width: 883px; left: 5px; height: 72px; padding-left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality system and...SuggestedWork at officeLocal areaImmediate startFlexible hours- Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This role is responsible for ensuring compliance with...Suggested
- ...Working Together, Persist with Passion. Who We’re Looking For: Laborie Medical Technologies is currently searching for a Regulatory Affairs Specialist to join our team in a hybrid role based out of the Portsmouth, NH or Minnetonka, MN offices. The Regulatory Affairs...SuggestedWorldwideFlexible hours
- ...Regulatory Affairs Specialist II - (RAS2.1) Company Description Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias and perform endovascular procedures. Its mission is the discovery, development and delivery...SuggestedWork at office
- ...The Science Team at Pride Health is hiring a "Regulatory Specialist" for a top materials science company. Key Responsibilities Manage U.S. product... ...regulated products. Collaborate with global Regulatory Affairs teams to facilitate regulatory submissions and approvals. Prepare...Suggested
$74.4k - $111.6k
...functional collaboration as we work together to engineer the extraordinary. This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product registration with global regulatory agencies to introduce...H1bLocal areaRemote workWorldwideFlexible hours$81.15k - $99.45k
...Summary Regulatory Affairs Specialist performs reviews and audits of certification related documentation, ensuring compliance to all quality management standards, governmental rules, regulations and requirements for the contract manufacturing of products. Fosters divisional...Full timeContract workLocal areaShift work$88k - $130k
...Regulatory Affairs Specialist Date: Aug 25, 2026 Location: Maple Grove, MN, US Company: Teleflex Expected Travel : Up to 10% Requisition ID :14019 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our...Temporary workWork at officeFlexible hours- ...Pride Health’s Science Team is hiring a Regulatory Specialist for a top materials science company in Maplewood, MN. The role focuses on U.S. product registrations, regulatory documentation, and collaboration with global teams to ensure timely submissions and approvals....Hourly pay
- .... • Conduct evaluations of chemical formulations to support regulatory compliance determinations. • Administer regulatory label and... ...Policy: Skills and Requirements • 4+ years of Regulatory Affairs experience in a corporate environment • Bachelor's degree with...
- ...Regulatory Affairs Specialist This role is ideal for a regulatory professional with strong experience in FDA, Health Canada, and EU medical device requirements. The Regulatory Affairs Specialist will maintain global registrations and technical documentation, support...Work at office
- ...a clinical-stage medical device company focused on transcatheter valve solutions for tricuspid regurgitation. We seek a Regulatory Affairs Specialist to support global regulatory activities across a growing portfolio and collaborate with Clinical, Quality, R&D, and Engineering...
- ...Socket.dev is seeking a Regulatory Affairs Specialist to support market authorizations and registrations for Scanlan products across worldwide markets. You will assist with design files, technical documentation, and product listings to ensure compliance and timely approvals...Worldwide
$81.15k - $99.45k
...A technology solutions provider in Winona, MN, seeks a Regulatory Affairs Specialist II. This role involves reviewing and auditing regulatory documentation to ensure compliance with quality standards and regulations for manufacturing. Key responsibilities include internal...- ...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Regulatory Affairs Specialist Regular Full-Time Scanlan International, Inc., St. Paul, MN, US The Regulatory Affairs Specialist will assist in...Full timeWork experience placementWork at officeWorldwide
- ...Abbott is seeking an individual contributor to perform specialized regulatory work, ensuring products meet regulatory requirements for... ...role requires a Bachelor’s degree and experience in regulatory affairs, with strong communication and organizational skills in a fast...
$74.4k - $111.6k
...collaboration as we work together to engineer the extraordinary.? This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product registration with global regulatory agencies to...Full timeH1bLocal areaImmediate startRemote workWorldwideFlexible hours- ...in medical technology.\This position will be instrumental in helping VDYNE achieve these ambitious goals. THE ROLE As a Regulatory Affairs Specialist at VDyne, you'll support regulatory operations and global clinical and commercial regulatory activities across an active...Work at officeShift work
- ...Abbott is seeking a Regulatory Affairs Specialist II to join our on-site team in Plymouth, MN. You will perform specialized analyses, prepare and review documentation for international regulatory submissions, primarily China, ensuring compliance with applicable regulations...
$94k - $150k
Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior Regulatory Affairs Specialist, UltrasoundThe Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities...Full timeWork at officeImmediate startWork visaRelocation package3 days per week- ...the right things and do things right 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 and ensure compliance...Full timeImmediate start
- ...supported in progressing - whatever your ambitions. About the role:We are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist to join our Interventional Oncology and Embolization division. In this role, you will play a pivotal role in supporting...Hourly payWork at officeLocal areaShift work3 days per week
- ...areas, extending our products into new geographies and high-growth adjacent markets.Under minimal supervision, the Senior Regulatory Affairs Specialist will plan, manage and implement regulatory submissions to the U.S. Food and Drug Administration (FDA), European Union...Hourly payWork experience placementWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- Laborie Medical Technologies is seeking a Regulatory Affairs Specialist for a hybrid role in Minnetonka, MN. You will support global product registrations and lifecycle maintenance for the US, Canada, Europe, and other regions. Responsibilities include preparing submissions...
- ...Senior Regulatory Affairs Specialist Work mode: Hybrid Onsite Location(s): Marlborough, MA, US, 01752 Additional Location(s): US-CA-Irvine; US-MN-Arden Hills; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance...Work at officeLocal areaRelocation3 days per week
- ...Principal Regulatory Affairs Specialist The Principal Regulatory Affairs Specialist is responsible for developing and implementing regulatory strategies across projects, processes, and/or products. This individual partners with internal stakeholders and external consultants...Worldwide
- ...Senior Regulatory Affairs Specialist Work mode: Hybrid Onsite Location(s): Marlborough, MA, US, 01752 Additional Location(s): US-MA-Marlborough; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific...Work at officeLocal area3 days per week
- ...Abbott Laboratories in the United States seeks a Principal Regulatory Affairs Specialist to join Abbott’s Vascular Division on-site in St. Paul, MN. The role focuses on global regulatory submissions, ensuring product compliance and timely market approvals. As an experienced...
$131k - $143k
...member of the Bracco Medical Technologies team has the power to make a difference......every day!About the RoleThe Principal Regulatory Affairs Specialist develops and executes regulatory strategies for medical device products, submissions, and lifecycle changes. This role...- ...focus is to revolutionize the standard of care in neuromodulation to positively impact patient’s lives. As a Principal Regulatory Affairs Specialist, you will provide Regulatory Affairs support for product development, sustaining engineering projects and compliance based...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!

