Abbott is seeking a Senior Specialist Regulatory Affairs to join the EMEAP regulatory affairs team in Witney. You will lead regulatory activities for new product introductions and on-market changes across the EMEAP region, coordinating submissions and liaising with Notified Bodies and authorities.
The role requires a Bachelor’s in a scientific field, strong MDR/IVDR experience, and excellent communication skills. Abbott offers a competitive salary and comprehensive benefits package.
Senior Regulatory Affairs Lead - Medical Devices (EMEAP) in Sydenham 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.
