GBUK Group is seeking a Validation Engineer to join the R&D/Quality team at the Head Office in Selby, North Yorkshire. You will lead validation activities across the product lifecycle, ensuring regulatory compliance and high-quality medical devices.
You will collaborate with R&D, Quality, Regulatory Affairs and Manufacturing, producing protocols and reports, reviewing processes, and supporting audits. Relevant ISO standards and a strong documentation focus are essential.
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Medical Device Validation Engineer - Quality & Compliance Lead in Selby employer: GBUK Group
GBUK Group is an exceptional employer that prioritises employee growth and development, with over 90% of our leadership team promoted from within. Our collaborative and supportive work culture fosters a sense of purpose, allowing you to make a real difference in patient care while enjoying a healthy work-life balance. Join us in Yorkshire, where your contributions are valued, and be part of a team that celebrates success and innovation in the medical device industry.
