Gina F.

Gina F. has a wealth of experience in the Regulatory Affairs and Quality Assurance field. Gina began their career in 1995 as a QC Environmental Monitoring Technician at B. Braun Medical, followed by a short assignment at Baxter Healthcare as a QC Microbiologist in 1996. In 1999, they became a QA Professional at Allergan, and in 2000, a QA Auditor at Baxter BioScience. In 2003, they joined DFE as a Regulatory Affairs & Quality Compliance Professional. From 2006 to 2014, they worked at Thomson Reuters in Paris, France as a Project/Editing Manager in Regulatory Affairs Intelligence. In 2015, they began working at the University of Southern California as a Regulatory Project Manager at the USC Norris Comprehensive Cancer Center - CISO. Gina then moved to Watkins-Conti Products, Inc. as a Senior Regulatory Project Manager.

Gina F. obtained a Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices from Northeastern University in 2017. Gina previously obtained a Bachelor of Science (B.S.) in Medical Microbiology and a Minor in Chemistry from California State University, Long Beach. Gina has also taken courses in Project Management at Cornell University and Nanotechnology and Nanomedicine at the University of Oxford, Department for Continuing Education. Gina has also obtained various certifications, including a Certified ScrumMaster\u00ae (CSM\u00ae) from the Scrum Alliance in 2018, a Project Management certification from Cornell University in 2018, a Medical Device Single Audit Program (MDSAP) Fundamentals and Readiness certification from BSI in 2017, a GS1 Standards Certificate from GS1 US in 2014, a Good Clinical Practice (GCP) certification from the Collaborative Institutional Training Initiative (CITI Program) at the University of Miami, a HIPAA Privacy Education certification from the University of Southern California, and a Human Subjects Research certification from the Collaborative Institutional Training Initiative (CITI Program) at the University of Miami.