Global Regulatory Affairs Specialist - Medical Devices

ELITechGroup is seeking a Regulatory Affairs Specialist in Logan, Utah. This role involves ensuring compliance with global regulatory requirements throughout the product lifecycle, from development to market surveillance. You'll collaborate with teams across R&D, Quality, and Marketing to support regulatory strategy and documentation.The ideal candidate has a Bachelor's degree and 2–5 years of regulatory affairs experience, particularly in the medical device field. Strong understanding of FDA and ISO regulations is essential.J-18808-Ljbffr