Global Regulatory Lead - Medical Devices
Smith & Nephew
Smith & Nephew in Mansfield, Massachusetts is seeking a Regulatory Affairs professional to shape regulatory strategy for innovative medical technologies. The role involves developing global regulatory strategies and managing submissions, with a strong focus on compliance across the product lifecycle. Qualified candidates will have a Bachelor's degree, at least 5 years of relevant experience, and proven success with FDA submissions. The position includes competitive compensation and comprehensive benefits aimed at work-life balance and personal well-being. #J-18808-Ljbffr Smith & Nephew
- Stark Pharma Solutions Inc. is seeking an experienced Regulatory Affairs Program Manager to lead a large-scale Medical Device Divestiture initiative. The role will oversee transfer of global regulatory registrations, submissions, and documentation to a newly established...RegulatoryMedical device
- Impellam Group is seeking a Regulatory Affairs Program Manager to lead the divestiture and transfer of regulatory documents to a new global medical device organization. You will drive the Regulatory Separation Plan, coordinate registrations, and manage ownership transfers...RegulatoryMedical device
- A professional staffing agency is seeking a Regulatory Affairs Specialist in Mansfield, MA. The ideal candidate will have experience... ...development teams and must be knowledgeable in FDA regulations and medical device submissions. This role involves providing regulatory...RegulatoryMedical device
- 6149-DePuy Synthes Products Inc. is looking for a Sr. Director, Regulatory Law to serve as the leading legal advisor on U.S. and global regulatory matters affecting medical devices. The ideal candidate will provide strategic counsel, ensuring compliance with regulatory...RegulatoryMedical device
- Johnson & Johnson MedTech is seeking a Sr. Director, Regulatory Law to oversee global regulatory activities in the orthopaedics medical device sector. You will support regulatory strategy, compliance, and innovation through expert legal counsel and collaboration with various...RegulatoryMedical device
- Johnson & Johnson, DePuy Synthes division, is recruiting a Sr. Director, Regulatory Law, to lead global regulatory activities across orthopedic medical devices. The role is based in Raynham, MA with scope across multiple geographies and entities. The position reports to...RegulatoryMedical device
$95k - $130k
...experienced, hands-on Quality Lead to lead and own the company's... ...System (QMS) within a regulated medical device environment and establish... ...specific QMS processes aligned with global QM while actively driving continuous improvement, regulatory readiness, and a culture of...RegulatoryMedical deviceFull timePart timeWork experience placementWork at office- Spectrum Vascular in Bridgewater, Massachusetts is looking for a Regulatory Affairs Specialist to support global regulatory submissions and ensure compliance with medical device regulations. The ideal candidate has a Bachelor's degree in a scientific field and 1-3 years...RegulatoryMedical device
- IntePros is seeking a Supply Planning Coordinator for a global medical device organization in Bridgewater, MA. This role involves coordinating inventory planning, maintaining accuracy, and supporting warehouse operations. Ideal candidates have 3-5 years of experience in...Medical device
$147.76k - $203.17k
Dormont Manufacturing Co is seeking a Regulatory Affairs Professional for their hybrid role in Walpole, MA. The candidate will prepare... ...a scientific field and at least two years of experience in medical devices or IVDs are required. This position offers a competitive...RegulatoryMedical device- A leading IT staffing firm is seeking a Regulatory Affairs Manager for a remote opportunity. The role involves ensuring compliance with FDA regulations... ...need a Bachelor’s degree, 5+ years of experience in medical device regulatory affairs, and strong leadership skills....RegulatoryMedical deviceRemote job
- ...Job title: Regulatory Affairs Specialist Location: Mansfield, MA Duration: 5+ months (possibility... ..., familiarity with FDA regulations for medical devices, submission experience of 510(k)s,... ...assessments, US letter to file (RAD), global regulatory strategy plans (GRSP),...RegulatoryMedical device
- ...Dormont Manufacturing Co is looking for a Regulatory Affairs (RA) Specialist in Bridgewater, Massachusetts. This role involves supporting regulatory submissions and compliance to ensure medical device products meet applicable regulatory requirements. The ideal candidate...RegulatoryMedical device
- Moderna seeks an Associate Director, Global Regulatory-CMC in Norwood, Massachusetts. This role involves coordinating regulatory CMC activities and developing strategies for transformative medicines. The ideal candidate will have at least 8 years in the biotech space, particularly...Regulatory
- BioSpace is seeking an Associate Director, Global Regulatory-CMC in Norwood, Massachusetts. This role involves coordinating regulatory activities and developing CMC strategies for product lifecycles. Candidates should possess a PhD in a relevant field and a minimum of 8...Regulatory
- ...seeking a Manager, Maintenance Excellence & AI Transformation to lead global AI-enabled maintenance initiatives across Facilities &... ...The role focuses on predictive maintenance, data integrity, regulatory alignment, and standardized maintenance across all sites. The...Regulatory
$178k - $307.05k
Position Summary The Sr. Director, Global Benefits COE - Orthopedics... ...global, regional, and local regulatory requirements and standards.... ...and business needs. Lead vendor strategy, including selection... ...such as healthcare, medical devices, or life sciences. Experience...RegulatoryMedical deviceLocal area- ...leadership for DePuy Synthes’ Global CRM technology platforms,... ...automation, customer data). Lead cross‑functional collaboration... ...data privacy, security, and regulatory requirements across global... ...regulated industries such as medical devices or life sciences. Other...RegulatoryMedical device
- ...through Staff Augmentation, Global Talent Management, Value Added... ...vacations, holidays, personal days, Medical, Dental and Vision insurance,... ...Insurance. Job Description Regulatory affairs with Technical Files,... ..., and/or auditing of medical device DHFs, Risk Management files,...RegulatoryMedical devicePermanent employment
- GLOBAL LEAD BUYER (SENIOR DIRECTOR) - Hybrid About the job GLOBAL LEAD BUYER (SENIOR DIRECTOR... ..., Professional Services, Scientific & Medical and Digital) leveraging Global... ...cost efficiency.In addition, activate the regulatory support through supplier collaboration,...Regulatory
$101.5k - $152.25k
...limits off living. Are you a regulatory affairs professional who... ...in supporting life changing medical technologies used by patients... ...to work collaboratively with global teams while shaping regulatory... ...for new and modified medical devices Preparing and managing regulatory...RegulatoryMedical deviceLocal areaFlexible hours- Regulatory Affairs Manager / Regulatory Affairs Specialist... ...Staff Augmentation, Global Talent Management, Value... ...In this role, you will lead the preparation, analysis... ...which may include device 510(k), IDEs, PMAs) and... ...preferred. 5+ years of medical device regulatory affairs...RegulatoryMedical devicePermanent employmentLocal area
- ...- Remote Opportunity - Regulatory Affairs Manager Established... ...Staff Augmentation, Global Talent Management,... ...In this role, you will lead the preparation, analysis... ...submissions which may include device 510(k), IDEs, PMAs) and... .... 5+ years of medical device regulatory affairs...RegulatoryMedical deviceRemote jobPermanent employmentTemporary workLocal area
- ...program risks. The ideal candidate has 5-7 years of experience in medical devices or consumer industries, with strong project management... ...offers an opportunity to work with diverse stakeholders and leads global projects while adhering to compliance standards. Candidates...Medical deviceContract work
- ...seeking an Associate Director, Benefits & Mobility, to lead the U.S.-based COE and provide governance for global benefits frameworks. This hands-on leadership role... ...aligning with Global Benefits Principles and regulatory requirements. The role oversees health & welfare,...Regulatory
- ...across manufacturing and facilities to advance decarbonization initiatives, tracks emissions with robust dashboards, and supports regulatory reporting. You will translate complex data into strategic actions and engage executives to align with business priorities. The...Regulatory
- A leading medical device company located in Massachusetts is seeking a Senior Engineer I, Quality Design Assurance to drive the quality development... ...-functional teams, leading risk analysis, and ensuring regulatory compliance throughout product development. Ideal candidates...RegulatoryMedical device
- ...through Staff Augmentation, Global Talent Management,... ...holidays, personal days, Medical, Dental and Vision... ...pneumatic compression devices used to prevent Deep Vein Thrombosis, a leading cause of morbidity in hospitals... ...Quality Assurance, Regulatory Affairs, Manufacturing,...RegulatoryMedical devicePermanent employment
- ...plans across multiple locations. The ideal candidate will possess a Bachelor's degree, 10+ years of leadership experience in the medical device industry, and strong communication skills. This position requires up to 50% travel and a strong presence on-site in Mansfield....Medical device
- Regulatory Affairs Program Manager (Medical Device Divestiture) Location: Raynham, MA / West Chester, PA / Palm Beach Gardens... ...Affairs Program Manager to lead a large-scale Medical Device Divestiture... ...role will manage the transfer of global regulatory registrations,...RegulatoryMedical device
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