IVDR Regulatory Affairs Specialist II – IVD

A leading global life sciences firm is seeking a Regulatory Affairs Specialist II to support the transition to EU In-Vitro Diagnostic Regulation (IVDR). The role focuses on revising documentation and ensuring compliance with regulatory standards. The ideal candidate will have a relevant Bachelor's degree and 3–5 years of experience in Regulatory Affairs or Quality Assurance within the IVD sector. Benefits include medical and vision insurance, as well as a 401(k).
This opening is for the IVDR Regulatory Affairs Specialist II – IVD role at Tucker Parker Smith Group (TPS Group). As a IVDR Regulatory Affairs Specialist II – IVD, you will play an important part at Tucker Parker Smith Group (TPS Group) in Dallas, TX, United States. We invite applications for the IVDR Regulatory Affairs Specialist II – IVD position located in Dallas, TX, United States.