Global Regulatory Lead – Medical Devices (EU MDR)

Medicareplus International Ltd in Greater London is seeking a Senior RA Specialist to oversee regulatory activities, ensuring compliance with medical device regulations. This role involves developing technical documentation, supporting product registrations, and collaborating across teams to ensure alignment with business objectives.

Ideal candidates will have over 5 years in the medical device sector, deep knowledge of EU MDR 2017/745, and a proven track record in regulatory submissions. The role offers competitive salary, generous holidays, and professional development opportunities.

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