Abbott is seeking a Senior Specialist Regulatory Affairs to join the EMEAP regulatory team. You will lead regulatory activities for new products and significant changes across Europe, the Middle East, Africa and Pakistan, coordinating submissions and interacting with Notified Bodies and regulatory contacts to ensure timely approvals.
You will develop strategies for cutting-edge medical devices and IVDs, oversee EU/UK Technical Files, and mentor junior staff while ensuring global regulatory
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Senior Regulatory Affairs Specialist – Med Devices (EMEA) in Witney employer: Abbott
Abbott Dundee is an exceptional employer that prioritises employee growth and development within a collaborative and safety-focused work culture. With a commitment to quality and continuous improvement, employees are empowered to contribute meaningfully in a GMP-compliant environment, ensuring the highest standards for healthcare products. The location offers a supportive atmosphere where attention to detail is valued, making it an ideal place for those seeking rewarding careers in manufacturing.
