ARC Belfast is seeking an experienced Regulatory affairs / Quality Assurance lead to deliver global compliance solutions for IVD devices and CDx products. You will prepare regulatory submissions, review quality systems, and advise across multiple markets, balancing client needs with regulatory expectations.
Requires 5+ years in a medical device GMP/GLP environment, engineering or science degree, and strong communication and analytical skills.
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Global IVD Regulatory Affairs Specialist employer: HIRANI
HIRANI is an exceptional employer located in Belfast, offering a dynamic work culture that fosters innovation and collaboration in the healthcare sector. Employees benefit from comprehensive professional development opportunities and a supportive environment that encourages growth and creativity, making it an ideal place for those passionate about leveraging Data and AI to drive meaningful change in healthcare.
