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
- ...As a Regulatory Affairs Specialist, you will drive hands‑on regulatory support to secure global marketing approvals for new products and maintain compliance for our existing... ...ensure strict compliance with applicable medical device advertising regulations. Regulatory Intelligence...Medical device
- ...Regulatory Affairs Specialist II - (RAS2.1) Company Description Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias... .... 3‑5 years’ experience in regulated medical device industry highly preferred. Knowledge of...Medical deviceWork at office
$74.4k - $111.6k
...Regulatory Affairs Specialist – Plymouth, MN We anticipate the application window for... ...for FDA and support global submissions. Maintain proficiency... ...the RA department and with device reviewers through oral and... ...affairs experience in the medical device industry OR advanced...Medical deviceTemporary workWorldwide- 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
- ...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
- Abbott Laboratories is seeking an individual for a specialized role, focused on regulatory compliance within the Medical Device sector. The role requires skills in preparing regulatory applications and a strong background in communication. Candidates should possess a Bachelor...Medical device
$61.3k - $122.7k
...Employees can qualify for free medical coverage in our Health... ...a passionate, experienced Regulatory Affairs Specialist II to join our team on-site... ...preparation and general support of global regulatory activities. This... ...implantable medical devices is preferred. What You’ll...Medical deviceWork at officeShift work$220k - $225k
...VP Global Quality and Regulatory Trelleborg Medical Solutions is seeking a VP Global Quality and Regulatory, based... ...impact the production of life-saving devices. Growth and advancement: Join... ...certification and/or Regulatory Affairs Certification (RAC) preferred...Medical deviceFixed term contract- ...Electrophysiology Division in Plymouth, MN. This role involves driving global marketing strategy and leading product launches for the Left... ...over 7 years of experience in product marketing within the medical device sector. We're looking for someone with leadership capabilities...Medical device
- ...sustainable franchise growth through marketing strategy and global launch ownership. Ideal candidates will have a Bachelor's degree... ...with at least 7 years of experience in product marketing and medical devices. Abbott offers a competitive salary and benefits including...Medical device
- ...Join Stryker as a Regulatory Affairs Specialist in Bloomington, MN supporting Trauma & Extremities .... ...regulatory activities, documentation, and global compliance across U.S. and... ...S. FDA regulations or international medical device regulations Experience working with...Medical deviceInternshipLocal area
$110.18k - $120k
...Regulatory Affairs Specialist Company: Heraeus Location: Fridley, MN Position Summary... ...responsible for initiating global regulatory strategies for... ...review post‑market changes for devices currently marketed to... ...cross functional peers on new medical device regulations, such as...Medical deviceFull timeRemote work$142.8k - $196.35k
## Principal Regulatory Affairs Specialist (Remote - United States)Applyremote type: Remotelocations:... ...the Dental Solutions business across global markets* Driving regulatory strategy... ...associated activities for assigned drug and medical device products* Leading or supporting...Medical deviceH1bRemote workRelocation packageFlexible hours$50.7k - $101.3k
...disease through breakthrough medical technologies in atrial fibrillation... ...of documentation for regulatory registration, ensuring products... ...domestic and international medical device regulations to ensure... ...Device industry. Regulatory Affairs Professionals Society Certification...Medical deviceFor contractorsWork experience placementWorldwide- Boston Scientific is hiring a Principal Regulatory Affairs Specialist in Maple Grove, MN, to lead regulatory strategy for a broad ablation portfolio... ...Affairs, strong technical writing, and a proven track record of global submissions #J-18808-Ljbffr Boston ScientificMedical device
$102.1k
Principal Regulatory Affairs Specialist - Advertising & Promotion (Ad Promo) Onsite Location(s): Maple... ...Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High... ...support and training materials for medical devices used in interventional cardiology. The...Medical deviceHourly payWork at officeLocal areaShift work3 days per week$88k - $130k
Position Summary This is a mid‑level Regulatory Affairs position responsible for integrating regulatory... ...changes to commercially distributed medical devices Conduct appropriate research to... ...Monitor the impact of changing and evolving global regulations on submissions, practices,...Medical deviceTemporary workWork at officeFlexible hours$102.1k - $194k
...week. Responsibilities Represent the Regulatory Affairs function on cross‑functional teams for... ...and prepare submissions for Class II medical devices. Create innovative regulatory pathways... ...product and project information to global regulatory teams and communicate international...Medical deviceWork at officeLocal areaOverseas3 days per week- ...Banner Recruiting is looking for a Senior Trade Compliance Specialist based in Minneapolis, Minnesota. The role ensures compliance with global trade regulations and focuses on providing technical classification expertise while supporting global operations. The ideal candidate...
- ...Katalyst CRO is seeking a highly skilled Medical Device Labeling Engineer based in Minneapolis, Minnesota. This position involves developing and maintaining labeling content, ensuring compliance with FDA and EU regulations, and leading labeling implementation activities...Medical device
$20 - $22 per hour
...Catheter Builder - Build Life-Changing Medical Devices. Grow Your Career. Work 4 Days a Week. $20 - $22/hour Schedule 1st Shift... ...clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit...Medical deviceWeekly payContract workTemporary workWorldwideWeekend workDay shift3 days per week$132.9k - $199.4k
Teleflex is looking for a Senior Global Product Manager to oversee the marketing for key technology categories within their Interventional... ...skills, and at least 5 years of relevant experience in the medical device space. The pay range for this role is between $132,900 - $199,...Medical device- ...Plymouth, MN. This full-time position plays a critical role in developing and executing hiring strategies within a high-growth medical device environment. The role includes managing the recruitment process, enhancing employer branding, and optimizing hiring practices....Medical deviceFull time
- ...Inc. in Plymouth, Minnesota, is looking for a professional to support import operations, ensuring compliant movement of goods across global markets. The role involves managing customs compliance and collaborating with cross-functional teams to improve operational...
$25 - $27 per hour
...and Associates is hiring a "Regulatory Specialist" for a top leading... ...involves working with regulatory affairs personnel across 80+ countries... ...or re-registering medical devices and pharmaceutical products... ...Employment Opportunity Pride Global and its affiliates are an equal...Medical deviceContract workLocal area- Stratasys is seeking a Sr. Import/Export Analyst to support global trade operations by ensuring compliance with import/export regulations. You will prepare and maintain documentation, coordinate international shipments, and analyze trade data for compliance and efficiencies...
- ...Title - Associate MDR/Vigilance Specialist Job Location - Mounds View,... ...- HM's Top Needs: 1. Nursing/medical backgrounds (ideally with... ...experience working with medical devices) 2. Biomedical engineering or... ...reaction data as required by regulatory agencies. Interface and collaborate...Medical deviceWork at office
- ...compliance activities related to complaint handling and ensuring adherence to regulatory requirements. Qualified candidates will have a Bachelor’s degree and at least 7 years in the medical device industry. A strong background in leadership and project management is...Medical deviceWork at office
$25 - $30 per hour
...Regulatory Specialist Our client, a leader in the healthcare industry, is seeking a Regulatory... ..., you will be part of the Regulatory Affairs department supporting global registration and re-registration processes for medical devices and pharmaceuticals. The ideal candidate...Medical deviceWeekly payTemporary workWork at officeLocal areaFlexible hours$100.9k - $151.3k
...Overview About Cretex Medical: Cretex Medical is a leading... ...and assemblies for the medical device industry. Our customers view... ...compliance with applicable regulatory requirements (e.g., FDA 21 CFR... ...Part 820, ISO 13485, and other global standards). Key...Medical deviceHourly payContract workTemporary workWork experience placementWork at officeLocal area
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