Flexible Hybrid Regulatory Specialist Jobs

A rapidly growing medical device organization is seeking a driven and detail‑oriented Regulatory Affairs Specialist II to join their Minneapolis team. This is an opportunity to step into a hands‑on role supporting innovative, life‑saving technologies while working closely with cross‑functional partners across product development, quality, and risk ...

A leading global medical device company is seeking a Regulatory Affairs Principal to support the review and approval of advertising, promotional, sales, and training materials for its interventional cardiology portfolio. This role applies a risk‑based regulatory mindset to ensure content is accurate, balanced, well‑substantiated, and compliant with...

Regulatory Affairs Consultant (Freelance) Location: Wavre, Belgium (Hybrid) Contract: 12 months (extendable) Start: July 2026 Key ResponsibilitiesDefine and implement US regulatory strategy to support FDA approval of a Class III device undergoing clinical investigation.Author, review, and maintain technical and regulatory documentation, including I...

EPM Scientific is working with an innovative medical device company in the oncology diagnostics space. The organisation develops cutting-edge technologies to support the detection and analysis of cancer cells, enabling more personalised treatment pathways.Role OverviewWe are seeking a Regulatory Affairs Manager to lead regulatory activities across ...

QA/RA Specialist: Dental/Additive Manufacturing Location: Eindhoven, Netherlands (Hybrid / Remote)Engagement: Part-time contract | Start ASAP | 6-12 months An innovative medical device company in Eindhoven is seeking an experienced Medior to Senior QA/RA professional to support regulatory and quality activities for dental and/or additive manufactu...