MedTech Regulatory Education Architect

Scarlet is seeking a Regulatory Quality Management Specialist to develop high-quality content for medical device innovators. The ideal candidate has over 3 years of experience in QMS implementation and regulatory compliance, specifically with EU MDR and ISO 13485. Responsibilities include designing training materials and leading discussions on auditing requirements. Compensation ranges from £60K to £80K. Join us in transforming healthcare accessibility.
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