Flexible Hybrid Regulatory Specialist Jobs
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Regulatory Affairs Consultant
We are looking for an experienced Regulatory Affairs Consultant to support MDR transition, risk management, and validation documentation activities within a highly regulated pharmaceutical/medical device environment. This 12‑month hybrid assignment is based in Antwerp, working 2-3 days on‑site. Key ResponsibilitiesUpdate and rewrite Risk Management...
Principal Regulatory Affairs Specialist Advertising & Promotion
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...
Freelance Consultant Software as a Medical Device (SaMD)
We're looking for an experienced freelance consultant to support regulatory and quality activities across a range of complex medical devices. This role suits someone who has worked with life‑sustaining, electromechanical, infusion, monitoring, renal, or surgical technologies and understands the demands of global compliance.What You'll DoDevelop reg...
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Regulatory Affairs Specialist (Autónomo)
Regulatory Affairs Specialist (Autónomo) - Medical Devices Location: Madrid, Spain (remote - 1 day per month travel)Length: 9 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 an ur...