Senior Regulatory Strategy Lead – Medical Devices (EMEAP)

Abbott is seeking a Regulatory Affairs specialist in Witney, UK, responsible for developing regulatory strategies for medical devices in the EMEAP region. You’ll oversee regulatory submissions, manage technical files, and act as a subject matter expert while ensuring compliance with EU regulations.

The ideal candidate will have a Bachelor’s degree in a scientific discipline and experience in regulatory or quality roles within the healthcare sector. Additional benefits include a competitive salary and tailor-made flexible benefits package.

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