Sarah Tomkins

WORK HISTORY

EDUCATION

ABOUT SARAH TOMKINS

With over 20 years experience in the Industry and 3.5 years of experience in regulatory affairs for medical devices, I am a Regulatory Affairs Manager at Convatec, a global leader in advanced wound care, infusion & ostomy solutions and continence care. In this role, I lead and manage regulatory affairs professionals responsible for projects impacting international markets, ensuring compliance with MDR, and other relevant regulations and standards. I oversee the change management process from a Regulatory perspective and provide guidance and support to internal and external stakeholders. Prior to joining Convatec, I worked as a Regulatory Affairs Manager and a RA Project Manager at Advanced Medical Solutions, where I was responsible for developing and executing regulatory strategies, submissions, and approvals for various medical device products. I have strong skills in MDR, quality systems, quality management, project management, and compliance, as well as a passion for delivering innovative and safe medical solutions that improve the lives of patients and healthcare professionals. I am eager to apply my expertise and knowledge to contribute to the mission and vision of Convatec, and to collaborate with a diverse and talented team of regulatory affairs professionals.