PJ Pardo is a seasoned professional in the medical device and pharmaceutical industries, currently serving as a Senior Medical Writer at Sight Sciences since May 2021. Pardo has extensive experience, having held key positions such as President/Senior Consultant at BDP Solutions, LLC since March 2005, where responsibilities include regulatory planning and compliance services. Previous roles also include EU MDR Medical Writer at ALKU, Senior Regulatory Affairs at Mentor Worldwide, LLC, Clinical Evaluation Scientist at Bannick LLC, and Medical Device RA/QA EU-MDR Management Consultant at Oriel STAT A MATRIX. Pardo was the Director of Regulatory and Clinical Affairs at LifeLine Scientifics, Inc. and the Director of Regulatory and Quality Management at Tutogen Medical, Inc. Pardo holds a PhD in Organization and Management from Capella University and multiple advanced degrees related to quality assurance and the sciences.
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