Regulatory Affairs Manager: EU MDR Strategy for Class III

Cure Talent is seeking a Regulatory Affairs Manager to lead the EU Regulatory Strategy for a new Class III medical device. This role involves defining approval pathways under MDR 2017/745 and leading regulatory strategy development from early stages to approval.

The ideal candidate will have proven experience in medical device regulatory affairs, specifically with Class III products, and will successfully collaborate across R&D and Clinical teams to ensure compliance and success of the regulatory program.

This high-impact role offers significant long-term progression potential within a globally recognized organization.

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