Abbott Laboratories is seeking a Senior Project Manager/Clinical Evaluation Reporting to lead CER activities for medical devices on-site in Santa Clara, Pleasanton, Atlanta, or St. Paul.
You will oversee CER writers, review Clinical Evaluation Reports, and support regulatory submissions under EU MDR 2017/745, MEDDEV, and CE marking requirements. The role requires a strong scientific writing background, at least 6 years in regulatory/clinical affairs, and the ability to drive cross-functional
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