Cure Talent are delighted to be partnered with an innovative IVD medical device company based in Manchester. They are expanding into new international markets and have an exciting opportunity for an RAQA Manager to take ownership of Quality and Regulatory functions.
As the RAQA Manager, you will be the subject matter expert for Quality and Regulatory Affairs within a small, technically focused team. This is a senior, hands-on role, responsible for maintaining ISO 13485 QMS and leading regulatory
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Senior RAQA Lead, ISO 13485 & IVDR | Global Compliance employer: Cure Talent
Join a leading global medical device company that is dedicated to innovation and excellence in life-saving technologies. As a Senior Regulatory Affairs Specialist, you will thrive in a collaborative work culture that values mentorship and continuous improvement, while enjoying opportunities for professional growth in a dynamic environment. Located in a vibrant area, this role offers the chance to make a meaningful impact on product portfolios and regulatory strategies, ensuring your contributions are recognised and valued.
