Senior Regulatory Affairs Lead – Medical Devices (EMEAP)

Abbott in Witney is seeking a Senior Specialist Regulatory Affairs to lead regulatory activities for new products and changes across the EMEAP region, coordinating with global teams to ensure timely approvals in Europe, Middle East, Africa and Pakistan.

You will build regulatory submissions, work with Notified Bodies and regulatory authorities, and mentor junior colleagues while advancing Abbott’s pipeline and product portfolio in a fast-paced healthcare environment.

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