Occupop is seeking a Regulatory Affairs Manager to lead and build the regulatory and quality function. This vital role ensures successful CE marking under EU MDR, allowing Boris to scale its products across the European market.The position requires strong expertise in regulatory compliance and quality management systems. Candidates should have 4-7 years of experience in medical device regulatory affairs, specifically with Class IIa/IIb devices, and possess a degree in a relevant field.This is a full-time position based in Dublin, offering a hybrid working model.
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