Global Regulatory Affairs Lead - Medical Devices
Boston Scientific Gruppe
Boston Scientific Gruppe is seeking a Regulatory Affairs professional to join their Interventional Oncology and Embolization team in Maple Grove, Minnesota. The role involves developing regulatory strategies and managing submissions for Class II medical devices, ensuring compliance with both US and EU regulations. The ideal candidate will have a Bachelor’s degree and at least 7 years of relevant experience, with proven project management and technical writing skills. The position follows a hybrid work model. #J-18808-Ljbffr Boston Scientific Gruppe
$132.9k - $199.4k
Teleflex is looking for a Senior Global Product Manager to oversee the marketing for key... ...based in Maple Grove, MN, and involves leading the global strategy for vascular closure... ...least 5 years of relevant experience in the medical device space. The pay range for this role is...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
$132.9k - $199.4k
Sr. Global Product Manager, Strategic Marketing... ...provider of medical technologies, Teleflex... ...medical devices used to diagnose and... ...peripheral intervention - leading both global... ...with R&D, Clinical, Regulatory, and Commercial teams... ...Regulatory, Clinical Affairs, Sales, Supply...Medical deviceTemporary workWork at officeFlexible hours- B Capital in Maple Grove, Minnesota, is seeking a Principal Regulatory Affairs Specialist to join their Interventional Oncology and Embolization team. This role is responsible for planning and managing regulatory submissions to FDA and EU, supporting new product development...Medical deviceWork at office3 days per week
- ...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
- Anteris® Technologies is a global structural heart company dedicated to revolutionizing... ...of aortic stenosis. Our Clinical and Regulatory Affairs teams play a critical role in... ...Clinical trial management within the medical device industry Roles in Clinical & Regulatory...Medical deviceTemporary workLocal areaWorldwideFlexible hours
- A global technology group is looking for a Project Manager to lead the development of cost models, track project performance, and translate user needs into requirements... ...field, with over 3 years of experience in the Medical Device industry and 2 years in a leadership role....Medical deviceFull time
$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
...Responsibilities Represent the Regulatory Affairs function on cross‑... ...prepare submissions for Class II medical devices. Create innovative... ...compliant updates to filings. Lead interactions with the U.S.... ...and project information to global regulatory teams and communicate...Medical deviceWork at officeLocal areaOverseas3 days per week- A global medical technology leader is seeking a Principal Regulatory Affairs Specialist in Maple Grove, MN. In this role, you will review and ensure compliance of advertising and promotional materials for medical devices. The position requires a minimum of 5 years in regulatory...Medical device3 days per week
- ...organization. About the Role: ~ Lead the development and execution of comprehensive... ...tools. ~ Understanding of medical devices and industry regulations. ~... ...work hours as necessary to engage with global teams and supply partners. Why Laborie...Medical deviceContract workFlexible hours
- ...Global Medical Director, Interventional Cardiology Work mode: Hybrid Onsite Location(s)... ...Research and Development (R&D), Quality, Regulatory Affairs and Commercial teams to support... ...internal teams to evaluate adverse events, device performance trends and emerging clinical...Medical deviceWork at officeWorldwide
- ...Principal Regulatory Affairs Specialist At Boston Scientific, we'll give... ...submissions for Class II medical devices. Create innovative regulatory... ...updates to filings. Lead interactions with the U.S.... ...and project information to global regulatory teams and communicate...Medical deviceWork at officeLocal areaWorldwide3 days per week
$32.24k
...Select how often (in days) to receive an alert: Create Alert Medical Device Assembler II Defined Term - All Shifts Onsite Location(s): Maple Grove, United States Diversity - Innovation - Caring - Global Collaboration - Winning Spirit- High Performance At Boston Scientific...Medical deviceHourly payWork experience placementWork at officeLocal areaRelocationRelocation packageAll shiftsMonday to FridayMonday to ThursdayFlexible hoursShift workNight shiftDay shiftAfternoon shift$88k - $130k
...Regulatory Affairs Specialist Date: Jun 26, 2026 Location: Maple Grove, MN, US Company... ...About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by... ...to commercially distributed medical devices • Conduct appropriate research to...Medical deviceTemporary workWork at officeFlexible hours- Bunzlcareers is seeking a Global Trade Compliance Manager in Maple Grove, MN, to oversee compliance for import and export operations.... ...the ability to collaborate across departments. Benefits include medical, dental, vision, and a 401k plan with company match. #J-18808-...
$117k
Loram is seeking a Manager, Payroll & HRIS to oversee global HR systems and payroll operations, ensuring accuracy and compliance. The... ...payroll processes. This role offers comprehensive benefits including medical, dental, vision insurance, and a competitive salary of $117,000...- ...Maple Grove, Minnesota. In this role, you will lead audits of metal suppliers to ensure compliance with regulatory requirements and Boston Scientific's standards.... ...and effective communication skills to influence global teams. The position offers competitive compensation...
$125.8k - $239k
Boston Scientific Gruppe is seeking a Global Senior Medical Education Manager to oversee the development and execution of a global medical education portfolio. This role requires strong program management skills and collaboration across various departments. As a key player...- Bunzl is seeking a highly skilled Global Trade Compliance Manager to oversee import and export compliance while developing and implementing... ...based in Maple Grove, MN or Morton Grove, IL. Benefits include medical, dental, vision, paid time off, and a 401K with a generous...
$125.8k - $239k
Boston Scientific seeks a Global Senior Medical Education Manager in Maple Grove, MN to lead a comprehensive medical education portfolio. This role focuses on developing high-quality educational programs for healthcare professionals while ensuring compliance and effectiveness...$167k - $315k
...Teleflex is a global provider of medical technologies, driven by our purpose to improve the health and... ...Teleflex develops innovative medical devices used to diagnose and treat coronary and... ...aligned with business growth objectives. Lead change management initiatives and...Medical deviceTemporary workFlexible hours- ...GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High... ...our employees experience every day.This Regulatory Affairs Principal role supports the review and... ...support and training materials for medical devices used in interventional cardiology. The...Medical deviceHourly payWork at officeLocal areaShift work3 days per week
- ...the role As a Fellow, Regulatory Affairs supporting the Intravascular... ..., clinically driven device programs. You will... ...influence and execute global regulatory strategies... ...responsibilities will include Lead the development,... ...technologies, complex medical devices, clinical...Medical deviceWork at officeLocal areaNight shift3 days per week
$58.2k - $110.5k
A leading medical solutions firm in Maple Grove is seeking a Quality Engineer I to improve manufacturing processes and ensure regulatory compliance. The ideal candidate will work closely with cross-functional teams, leading investigations and quality projects. Applicants...Medical device- Teleflex is seeking a mid-level Regulatory Affairs professional to manage regulatory processes throughout the product lifecycle. This role... ...The ideal candidate will have 2-5 years of experience in medical devices, strong analytical skills, and proficiency in Microsoft...Medical deviceWork at office
- ..., focusing on innovative digital strategies and product management. Qualifications include 10+ years in marketing, 5+ years in Medical Devices, and a BA/BS degree. The position requires ~30% travel and follows a hybrid work model, requiring at least three days in the office...Medical deviceWork at office
- ...Maple Grove, Minnesota, is seeking a qualified Quality Assurance Specialist to ensure production and process control compliance in medical device manufacturing. Responsibilities include monitoring production staff, performing Device History Record reviews, and providing...Medical device
- ...Grove, MN, is hiring a Quality Assurance Engineer responsible for ensuring compliance throughout the manufacturing process of medical devices. The role involves oversight of documentation, audits, and quality metrics, requiring strong communication skills and attention...Medical device
$110.18k - $120k
...Regulatory Affairs Specialist Company: Heraeus Location: Fridley, MN Position... ...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
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