CMR Surgical Ltd in Cambridge is seeking a Regulatory Affairs professional to support the development and execution of regulatory strategies for medical devices, focusing on EU MDR and US FDA requirements. This role ensures submissions meet regulatory expectations and integrates requirements across product development.
You will collaborate with R&D, Quality, Clinical and Manufacturing teams to gather data, prepare submissions such as 510(k)s and EU filings, and respond to questions from Notified
#J-18808-LjbffrGlobal Regulatory Affairs Specialist - EU MDR & FDA in Cambridge employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
