Masimo Irvine, CA is seeking a Senior Medical Writer to develop clinical evaluation reports (CERs) and post-market surveillance (PMS) reports in compliance with EU MDR and global standards. You will lead literature reviews, appraise evidence, and collaborate with Scientific Affairs, Clinical Research, Regulatory Affairs, Engineering, and Marketing to support product portfolio compliance.
You will report to the Sr Director, Scientific Affairs & Research, and this is an on-site role in Irvine, CA.
