Amaris Consulting in Bothell, WA seeks dynamic Life Sciences consultants to help remediate design control gaps and drive regulatory-compliant verification across medical device families. You will author and update DFMEA/PFMEA/UFMEA, manage risk analyses, and ensure traceability from business needs to verification evidence, using leading ALM tools.
Candidates bring 3–7+ years in regulated medical device development, strong writing and cross-functional collaboration skills, and fluency in English
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