Global Regulatory Lead, Oncology Diagnostics

A leading precision oncology company is seeking a Sr. Regulatory Affairs Specialist to develop and implement regulatory strategies for IVD and Companion Diagnostics products. This role requires collaboration with cross-functional teams to support product registration and approvals. Candidates should have an advanced degree in life sciences and at least 2 years of experience in regulatory affairs or related fields. The company offers competitive salary and a hybrid work model. #J-18808-Ljbffr