Flexible Hybrid Regulatory Specialist Jobs

Job Title: Senior Regulatory Affairs Specialist Supervisor/Manager Title: Senior Manager, Regulatory AffairsJob Description Summary: Responsible for timely preparation and submission of organized, scientifically valid global regulatory affairs submissions (clinical, pre- and post-market applications), query responses, and correspondence tracking. M...

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 ...

Regulatory Affairs Specialist (Autónomo) - Medical Devices Location: Barcelona, Spain (remote - 2 days per month travel)Length: 12 months (possibility of extension)Start Date: ASAP We are partnered with a growing medical device manufacturer seeking an experienced Regulatory Affairs Specialist (Autónomo contractor) for a 9‑month engagement. This is ...

Location: Brussels, Belgium (1-2 days per week on site)Start Date: Ideally ASAPContact: 12 months (freelance engagement) About the RoleWe're looking for an experienced consultant to advise on regulatory and quality strategies for software-driven medical technologies. This role is ideal for someone who understands the complexities of compliance for ...

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...