Global Regulatory Affairs Specialist - Medical Devices
Abbott
Abbott's Electrophysiology business in Plymouth, Minnesota, seeks a regulatory affairs specialist to prepare documentation for regulatory submissions in heart disease treatment. The role involves collaborating with teams, ensuring compliance with FDA standards, and supporting product market entry. The ideal candidate will have a Bachelor’s Degree and strong communication and organizational skills. Abbott offers comprehensive career development and competitive benefits, including medical coverage and retirement plans. #J-18808-Ljbffr Abbott
- 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,... ...engineering and 1-3 years’ medical device regulatory experience are required...Medical device
- Integer Holdings is seeking a senior regulatory affairs professional to develop and manage US and international regulatory strategies for medical device submissions. You will prepare submissions, interact with FDA/other agencies, and serve as a cross‑functional regulatory...Medical device
- Laborie is seeking a Regulatory Affairs Specialist to join our team in a hybrid role based out of Minnetonka, MN or Portsmouth, NH. You will support global product registration, approvals, and lifecycle management across major markets including the US, Canada, Europe,...Medical device
- AtriCure, Inc. in Minnesota seeks a Senior Regulatory Affairs Specialist to originate and maintain marketing... ...submit 510(k), PMA supplements, and global filings, while guiding regulatory... ...requires regulatory expertise for medical devices, strong technical writing, and...Medical device
- Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within... ...possess deep knowledge of U.S. and international medical device regulations, strong analytical capabilities, and...Medical device
$92k - $138k
...start here. Medtronic is a global leader in healthcare technology... ...— developing innovative medical technologies that improve... ...looking for a passionate Senior Regulatory Affairs Specialist who has direct experience... ...and changes to existing devices and documentation. Support...Medical deviceFull timeH1bLocal areaImmediate startWorldwideFlexible hours- Abbott is seeking a Regulatory Affairs Specialist II to work on-site in Plymouth, MN. This role requires strong attention... ...skills while preparing and supporting global regulatory activities for implantable medical devices. With 2-3 years of experience in a regulated...Medical device
- AtriCure, Inc. seeks a Senior Regulatory Affairs Specialist to originate and maintain marketing privileges across US and international markets. This role will prepare submissions and support regulatory strategies for new product development and post-market changes. You...Medical device
- Senior Regulatory Affairs Specialist - Medical Devices About the Role We are seeking a Senior Regulatory Affairs Specialist to support global regulatory activities for medical devices. This role partners with cross‑functional teams to develop regulatory strategies, prepare...Medical device
- ...technologies. The company seeks professionals for Clinical & Regulatory Affairs roles to support clinical research and regulatory... ...development opportunities. Candidates with experience in Class III medical devices are especially encouraged to apply. #J-18808-Ljbffr...Medical device
- Job Title: Regulatory Affairs Specialist II Location: Minneapolis, MN 55401, US (Primary) Education:... ...Responsibilities Evaluates potential global regulatory pathways for US, EU, and... ...3-5 years' experience in regulated medical device industry highly preferred. Knowledge...Medical deviceFull timeWork at office
$131k - $143k
Why Join Bracco Medical Technologies? At Bracco Medical... ...where experienced regulatory professionals can influence global product strategy, partner... ...The Principal Regulatory Affairs Specialist develops and executes regulatory... ...strategies for medical device products, submissions,...Medical device$61.3k - $122.7k
...Regulatory Affairs Specialist II Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-... ...leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our...Medical deviceFlexible hours- ...the healthcare industry, is seeking a Regulatory Affairs Specialist to join their team. As a Regulatory... ...Affairs Department supporting global post-market compliance activities. The... ...Regulatory Affairs and/or Quality within the medical device, healthcare, or life sciences...Medical deviceWeekly payTemporary workFlexible hours
$61.3k - $122.7k
...Abbott Regulatory Affairs Specialist II Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of... ...leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our...Medical deviceWork at office$94k - $150k
...Senior Regulatory Affairs Specialist The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams... ...Technical Files, Declarations of Conformity, and Medical Device Licensesfor various global markets. Support cross-functional teams with...Medical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week$50.7k - $101.3k
Abbott is a global healthcare leader that helps people live more... ...products in diagnostics, medical devices, nutritionals and branded generic... ...of documentation for regulatory registration, ensuring products... ...Device industry. Regulatory Affairs Professionals Society Certification...Medical deviceFor contractorsWork experience placementWorldwide$74.4k - $111.6k
...Regulatory Affairs Specialist Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate... ...developing innovative medical technologies that improve... ...and changes to existing devices and documentation. Providing...Medical deviceH1bWork at officeLocal areaImmediate startWorldwideFlexible hours$92k - $138k
...Senior Regulatory Affairs Specialist Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission... ...developing innovative medical technologies that improve... ...labeling and changes to existing devices and documentation....Medical deviceTemporary workH1bLocal areaImmediate startWorldwideFlexible hours$85k - $104k
...Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment... ...FUNCTIONS OF THE POSITION: Support global regulatory pre-market applications for... ...Change Control) Work with Regulatory Affairs staff, engineers and technical experts...Medical deviceContract workTemporary workFor contractorsFor subcontractorWork at officeLocal areaRemote workWorldwide$120.49k - $192.78k
...Principal Regulatory Affairs Specialist Join RespirTech's team in Plymouth, MN as... ...you will develop and execute global regulatory strategies for... ...innovative airway clearance therapy devices, enhancing product... ...experience within FDA regulated Medical Device environments, with a...Medical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week- Abbott seeks a Senior Product Manager for Global Upstream Marketing in the TAVI portfolio. You will lead global strategy, shape the... ...thinking, excellent communication, and experience in medical devices or healthcare marketing at a global scale. #J-18808-Ljbffr AbbottMedical device
$129.5k - $203.5k
...that are essential in everyday technology devices from smartphones to electric vehicles, or... ...like Spectrum and Liveo, we advance global health through innovation.We are hiring a... ...skillsPreferred ExperienceCardiovascular or medical device market experienceGlobal / cross-cultural...Medical deviceRemote work$200k - $275k
A medical technology company based in Plymouth, Minnesota, is seeking a Global Software Leader for Acute Products/Devices. This role requires significant experience in device software engineering, managing a globally distributed team, and a strong understanding of medical...Medical device- ...in Plymouth, MN is seeking an External Manufacturing Leader to drive end-to-end management of a global third-party manufacturing network in a highly regulated medical device environment. You will lead CMOs, strengthen infrastructure, and ensure supply continuity, quality...Medical device
- Medtronic plc is seeking a Senior Regulatory Affairs Specialist to lead worldwide product registrations... ...to the FDA, EU MDR, and other global agencies, and collaborating with cross... ...global regulatory strategy for high-risk medical devices, leveraging your experience to...Medical deviceWorldwide
- Philips seeks an External Manufacturing Leader to drive execution across a global third-party manufacturing network in a highly regulated medical device environment. You will strengthen infrastructure, elevate operational rigor, and build scalable processes across a global...Medical device
$165.55k - $260.15k
...essential in everyday technology devices from smartphones to electric... ...processes across Spectrum’s global Healthcare manufacturing... ...meet critical-to-quality (CTQ), regulatory, and customer requirements.Operational... ...experience, ideally in the medical device manufacturing industry...Medical deviceFlexible hours- 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...Medical device
$135k - $145k
...- innovating at the speed of life.As a global leader in clinical diagnostics, Beckman... ...partnering constructively with Quality, Regulatory, and Operations stakeholders.The... ...and technology transfer projects in the Medical Device or Diagnostics regulatory environment,...Medical deviceFull time
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