Global Medical Device Regulatory Affairs Strategist

A leading technology company in South Carolina is seeking a Medical Device Regulatory Affairs Strategist. This role involves collaborating with engineering teams on the product lifecycle of software applications within the healthcare sector. Responsibilities include ensuring compliance with regulatory standards and conducting audits. The ideal candidate will possess experience in regulatory affairs and skills in risk assessment and compliance management. A comprehensive benefits package is provided, including medical insurance and a 401(k) plan. #J-18808-Ljbffr