Global IVD Regulatory Affairs Lead

A global medical technology company in San Jose is seeking a Regulatory Affairs professional to develop and execute regulatory strategies for in vitro diagnostic devices. The ideal candidate should have a Bachelor’s degree in biological sciences and a minimum of 3 years' experience in regulatory affairs within the device or pharmaceutical industries. Strong project management and communication skills are essential. Join a team that values inclusion, growth, and a supportive culture with competitive compensation and benefits. #J-18808-Ljbffr