Jason Gillette, ACNS, BSM, CNPRx, CDR, DRIC, CIA, DR3PL

Jason Gillette has over 20 years of experience in the pharmaceutical and medical industries. Jason began their career in 1998 as an Inventory Control Coordinator at The Mentholatum Company, Inc. In 2003, they moved to Cooper Turbocompressor, Inc. as an Aftermarket Planner Specialist. In 2007, they became a Compliance Coordinator at PATTERSON MEDICAL SUPPLY, INC. where they were responsible for analyzing and implementing State, local, and Federal Regulations. In 2012, they moved to International Pharma Packaging & Distribution as a Regulatory Compliance Coordinator where they were the primary contact with Board of Pharmacies, initiated and renewed licenses and registrations. In 2014, they became the Regional Quality Systems Manager at Fresenius Medical Care North America where they were responsible for directing and maintaining a compliant FDA/ State Board of Pharmacy Quality System. In 2015, they became the Vice President of Regulatory Compliance at Westminster Pharmaceuticals, LLC. In 2017, they moved to LSPediA - Life Sciences Solutions as a Project Manager where they were responsible for engineering activities related to the design, development, configuration, training, and deployment of FDA DSCSA serialization programs. In 2018, they became the Executive Vice President of Regulatory Compliance at Integra Pharma Solutions where they utilized transferable skills to achieve retail pharmacy acquisition via Risk Gap Analysis. Currently, they are a Sales Executive at Qualityze Inc. where they are driving passion of bringing next generation technology into the quality space.

Jason Gillette has a diverse educational background. Jason obtained a Diploma in Precision Machining from Erie I BOCES in 1998-1999, an Associate of Occupational Studies in Computer Network Systems from ITT Technical Institute in 2000-2002, a Certificate in Microsoft Office Suite from Erie Community College in 2000, a Certificate in OSHA 511: Occupational Safety and Health Standards for General Industry from University at Buffalo in 2007, a Bachelor of Science in Management from Houghton University in 2005-2009, a Certificate in Becoming a Leader in the Life Sciences from Millard Fillmore College, University at Buffalo in 2009, a Certificate in Bio-Manufacturing Training from Erie Community College in 2009, and a Graduate Certificate in REMeDI (Regulatory Environment of Medical Devices & Implants) from Millard Fillmore College, University at Buffalo in 2010-2011. In addition, Jason Gillette holds various certifications, such as HIPAA Certified from PAAS National, Inc. in 2020, Health Care Fraud, Waste and Abuse FWA Certified (Combating Medicare Parts C and D Fraud, Waste, and Abuse Medicare Parts C and D General Compliance) from PAAS National, Inc. in 2020, GS1 Standards for DSCSA Suppliers Online Certificate from GS1 US in 2017, CNPRx (Certified National Pharmaceutical Rep.) from National Association of Pharmaceutical Sales Rep in 2011, DRIC (Drug Wholesaler Designated Rep. In-Charge) from California Board of Pharmacy in 2010, CDR (Certified Designated Rep.) from Florida Department of Business & Professional Regulation in 2009, ISO 9001: 2000 Internal Auditor with Medical Device Focus Certificate (ISO 13485:2003) from AQS Management Systems, Inc. (RABQSA Certified) in 2008, Designated Representative - 3PL from California Board of Pharmacy, Device Establishment Registration and Listing from CDRH Learn, FDA’s Center for Devices and Radiological Health (CDRH), Export Certificates for Medical Devices from CDRH Learn, FDA’s Center for Devices and Radiological Health, Good Clinical Practice 101: An Introduction from CDRH Learn, FDA’s Center for Devices and Radiological Health (CDRH), Introduction to Medical Device Recalls: Industry Responsibilities from CDRH Learn, FDA’s Center for Devices and Radiological Health (CDRH), Overview of Regulatory Requirements: Medical Devices from CDRH Learn,