Global Regulatory Affairs Lead – Medical Devices (Hybrid)

A health technology company is seeking a Senior Regulatory Affairs Specialist to guide regulatory strategy for medical devices, ensuring compliance with domestic and international regulations. This role includes preparing regulatory submissions, interacting with authorities, and advising on product lifecycle compliance. The ideal candidate will have a Bachelor’s degree and a minimum of 5 years in Regulatory Affairs. The position offers a hybrid work model between Palo Alto, CA and Guilford, CT, with a competitive salary range of $125,000 - $145,000.
#J-18808-Ljbffr