Bioventus is seeking a Regulatory Affairs professional to join our team and support registrations across multiple regions. The role focuses on ensuring compliance for electromechanical and implantable medical devices, coordinating with global teams and regulatory bodies.
You will handle registrations, certifications, and prepare documentation, reporting to the Manager Regulatory Affairs, with a strong emphasis on clear communication, attention to detail, and cross-time-zone collaboration.
#J-18808-LjbffrGlobal Regulatory Affairs Lead - Medical Devices employer: Bioventus
Bioventus is an exceptional employer that prioritises employee growth and development within the dynamic medical device sector. With a collaborative work culture and a commitment to maximising both profitability and patient impact, employees benefit from extensive training opportunities and the chance to lead innovative sales strategies across the UK and South. The role offers the unique advantage of engaging directly with NHS and private hospitals, making a meaningful difference in healthcare while enjoying a supportive team environment.
