Global Regulatory Affairs Lead - Medical Devices

A leading medical device company in California is seeking a Sr. Regulatory Affairs Specialist to develop and implement regulatory strategies for medical devices. This role involves preparing submissions, ensuring compliance with global regulations, and collaborating with cross-functional teams. Candidates should have 5-7 years of experience in regulatory affairs specific to medical devices and a Bachelor's or Master's degree in a relevant field. This position is fully onsite and offers competitive compensation and benefits. #J-18808-Ljbffr