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Kimberly Meade has a strong background in quality and regulatory compliance, with extensive experience in various industries. Kimberly currently serves as the Executive Director of Quality & Regulatory Compliance at ProSciento, Inc., where they are responsible for ensuring compliance with quality standards and regulatory requirements. Prior to this role, they held positions as Director of Quality at ProSciento, Inc. and Associate Director of Quality at Abbott.

Before joining Abbott, Meade worked at Merge Healthcare as the Manager of Regulatory Affairs/Quality Assurance, where they managed and facilitated regulatory compliance and oversaw the Quality Management System. Kimberly also has experience at CareFusion as a Manager of QC Services, where they managed strategic oversight and leadership direction within the Quality and Regulatory Affairs function.

Earlier in their career, Meade worked at DR Systems Inc. as a Manager of Quality Assurance Regulatory Compliance, where they facilitated the overall Corporate Quality System and maintained compliance with FDA regulations. Kimberly also held the position of Manager of Quality Assurance at Copper Mountain Networks, where they managed a team and was responsible for quality systems and ISO 9001 certification.

Meade's work experience began at Hughes Network Systems as a Quality Engineer, where they implemented SPC charts and conducted ISO 9000 internal audits.

Overall, Meade's work experience demonstrates their expertise in quality and regulatory compliance, as well as their ability to effectively manage and improve quality management systems.

Kimberly Meade has a diverse education history in the field of service and health care quality assurance. In 1985 to 1987, they obtained a B.A. in Business Administration from National University. Kimberly later pursued multiple professional certificates in various fields. From 1995 to 1997, they completed a Professional Certification in Competitive Manufacturing at UC San Diego Extended Studies. In 2000 to 2001, they obtained a Professional Certificate in Quality Management, and in 2001 to 2002, they received a Professional Certificate in Project Management, both from UC San Diego Extended Studies as well. Additionally, they completed a Professional Certificate in Quality Assurance and Control for Drugs and Biologics from UC San Diego Extended Studies from 2016 to 2017. In 2020, they pursued a Professional Certificate in Clinical Trials Administration from UC San Diego Extended Studies as well. Moreover, they earned an MSQA (Master of Science in Quality Assurance) degree from California State University-Dominguez Hills from 2010 to 2013.

Kimberly Meade also holds several additional certifications. In 2007, they achieved the ISO 13485:2003 RABQSA Certified Lead Auditor certification from RABQSA. In 2008, they obtained the Certified Quality Auditor certification from ASQ - World Headquarters. Kimberly also holds the Regulatory Affairs Certification (RAC) - Medical Device from the Regulatory Affairs Professionals Society (RAPS), obtained in 2019. Lastly, they have achieved the Registered Quality Assurance Professional in Good Clinical Practice (RQAP-GCP) certification from the Society of Quality Assurance in October 2021.