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
- 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
- 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
- VDYNE is 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...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
$107.2k - $160.8k
...left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for day-to-day regulatory... ...experience in regulatory affairs in Medical Device industryFamiliarity with FDA and EU... ...ethical integrityOpen-minded with a global mindsetEmbraces cultural differences...Medical deviceWork at officeLocal areaImmediate startFlexible hours$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- 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
$70k - $110k
...Shift Type Job Title Regulatory Affairs Specialist II Education Bachelor's Degree Location... ...: Stereotaxis is the global leader in innovative robotic technologies... ...3-5 years' experience in regulated medical device industry highly preferred. • Knowledge...Medical deviceFull timeWork at officeShift work$94k - $150k
...Senior Regulatory Affairs Specialist, Ultrasound The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory... ...Technical Files, Declarations of Conformity, and Medical Device Licenses—for various global markets. Support cross-functional teams with...Medical deviceFull timeWork at officeLocal areaWork visaRelocation package3 days per week- Saluda Medical is a commercial‑stage medical device company focused on developing treatments for chronic neurological... ...’s lives. As a Principal Regulatory Affairs Specialist, you will provide Regulatory... ...regulatory strategies, prepare global regulatory submissions and...Medical device
- Saluda Medical is a commercial‑stage medical device company focused on developing treatments for chronic neurological... ...Reporting to the Sr. Director, Regulatory Affairs, the Senior Regulatory Affairs Specialist will provide input to global regulatory strategies and support...Medical device
$61.3k - $122.7k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in...Medical deviceFlexible hours$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$61.3k - $122.7k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in...Medical deviceFor contractorsWork experience placementWorldwide$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$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
- 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
- ...Regulatory Affairs Specialist Medtronic is seeking a Regulatory Affairs Specialist to support the... ...provide regulatory support on a range of medical devices focusing on a diverse line of... ...Regulatory support will focus on sustaining globalization, international submissions,...Medical deviceFlexible hours
$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- ...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...Medical deviceWork at office
- 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
- ...Senior Regulatory Affairs Specialist Work mode: Hybrid Onsite Location(s): Marlborough... ...- Innovation - Caring - Global Collaboration - Winning... ...growing active implantable device portfolio. This role will be... ...Affairs experience in the medical industry Prior experience...Medical deviceWork at officeLocal areaRelocation3 days per week
$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- ...Job Title: Regulatory Affairs Specialist III Location: Maplewood, MN Duration: 18 Months+ Pay... ...innovation, and continuous improvement. Our global organization enables our customers... ..., bioprocessing, diagnostics, medical device, pharmaceutical, or chemical products...Medical deviceMonday to FridayFlexible hours
$74.4k - $111.6k
...start here. Medtronic is a global leader in healthcare technology... ...- developing innovative medical technologies that improve... ...Medtronic is seeking a Regulatory Affairs Specialist to support the Wound Management... ...support on a range of medical devices focusing on a diverse line...Medical deviceFull timeH1bWork at officeLocal areaImmediate startFlexible hours- Principal Regulatory Affairs Specialist The Principal Regulatory Affairs Specialist... ...submissions and changes to existing devices, including development of... ...registrations for global product growth and market expansion... ...7+ years of experience in medical device Regulatory Affairs....Medical deviceWorldwide
- ...Who We’re Looking For: Laborie Medical Technologies is currently searching for a Regulatory Affairs Specialist to join our team in a hybrid... ...Specialist will support global product registration, approval... ...Regulatory Affairs in the medical device industry 1-3 years'...Medical deviceWorldwideFlexible hours
$80.9k - $127.05k
...time 20186058 What Regulatory Affairs contributes to... ...enable pharmaceutical, medical and biotechnology companies... ...Regulatory Affairs Specialist supports the Medical... ...registrations, developing global regulatory strategies... ...and medical device requirements. Monitor...Medical deviceFull timeTemporary workWork experience placementLocal areaImmediate startRemote workFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Global Regulatory Affairs Specialist - Medical Devices. Be the first to apply!
- regulatory compliance analyst Minneapolis, MN
- medicare compliance specialist Minneapolis, MN
- regulatory analyst Minneapolis, MN
- legal compliance officer Minneapolis, MN
- regulatory specialist Minneapolis, MN
- risk and compliance analyst Minneapolis, MN
- information security compliance analyst Minneapolis, MN
- aml compliance analyst Minneapolis, MN
- regulatory compliance associate Minneapolis, MN
- compliance officer Minneapolis, MN

