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Lead Regulatory Affairs Specialist
Barcelona€50,000 - €65,000 EUR a year

Lead Regulatory Affairs Specialist Barcelona - Flexible Hybrid Working €50,000-€65,000 Are you an experienced Regulatory Affairs professional within the medical device industry?Are you looking for a role where you can take ownership of Regulatory Affairs activities, work on innovative robotic medical technologies, and play a key role in supporting ...

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Director / Senior Regulatory Affairs Leader (US)
Playa Vista$233,750 USD a year

Director, Regulatory Affairs (US)We are seeking an experienced Regulatory Affairs leader to establish and lead the US regulatory function for a growing medical device company. This individual will be responsible for FDA engagement, regulatory submissions, compliance strategy, and supporting market expansion across the US.ResponsibilitiesBuild and l...

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Regulatory Affairs Manager
Barcelona€55,000 - €65,000 EUR a year

Regulatory Affairs Specialist Barcelona - Hybrid Working €55,000-€65,000 Are you an experienced Regulatory Affairs professional within the medical device industry?Are you looking for a role where you can take ownership of Regulatory Affairs activities, work on innovative robotic medical technologies, and play a key role in supporting international ...

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Selby Jennings Start Your Career In Recruitment
Senior Regulatory Affairs Specialist
Negotiable

EPM Scientific are partnered with a Global Diagnostics Manufacturer to hire a Sr. Regulatory Affairs Specialist primarily supporting Performance Study Applications for CDx programs to EU Competent Authorities and/or MHRA via CRO.This is a 12 month, full time contract, starting ASAP. Remote with occasional on site presence in the north of England id...

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Senior Manager Regulatory Affairs Ad/Promo Medical Device
MinneapolisNegotiable

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

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