Jennifer Saylor is a highly experienced professional in regulatory affairs and post-market surveillance, currently serving as the Post Market Surveillance Manager at OriGen Biomedical since February 2023. Prior to this role, Jennifer held various positions including Senior Regulatory Affairs Specialist at Smith+Nephew, where responsibilities included managing post-market surveillance activities, and as a PMS Consultant at EG Life Sciences. Additional experience includes working as a Post Market Surveillance Consultant at Validant, where legal and complaint review tasks were performed, and as a Quality Engineer at Vapotherm, focusing on device failure investigations and complaint handling. Earlier career roles include a Design Control Specialist at DENTSPLY International, an Environmental Educator with Delaware State Parks, and internships at Honeywell International and MCV Physical Therapy Lab. Jennifer holds a B.S. in Biomedical Engineering from Virginia Commonwealth University and a Lean/Six Sigma Certificate from Villanova University.
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