Smith+Naphew, based in Hull, is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities for wound management products and ensure global compliance. The role collaborates with cross-functional teams to guide development, changes, and launches, driving registrations and approvals worldwide.
You will work in a hybrid setup, ensuring adherence to ISO 13485, FDA 21 CFR Part 820, and cGMP/cGDP standards while supporting continuous improvement and knowledge sharing across the team.
#J-18808-LjbffrSenior Regulatory Affairs Lead – Global Medical Devices 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.
