Jessica Montejo Mt, Mba, Rac-Devices

Jessica Montejo has a diverse work experience in the field of regulatory affairs and quality management. Jessica is currently working as the Director of Regulatory and Quality at Alma Lasers North America since October 2019. Prior to this, they served as a Regulatory Affairs Project Manager at Sysmex America, Inc. from March 2016 to October 2019. Before that, they worked as a Senior Regulatory Affairs Specialist at Medline Industries, Inc. from November 2014 to March 2016. Jessica also has experience working at Baxter International Inc. as a Sr. Regulatory Affairs Associate from July 2012 to April 2014. Moreover, they worked as a Sr. Regulatory Affairs Associate at Teleflex Medical OEM from September 2011 to July 2012. In addition, they have worked in quality management roles at Baxter Healthcare, where they served as a Quality Associate III from February 2010 to September 2011, a Quality Associate II from September 2008 to February 2010, a Quality Associate I from March 2008 to September 2008, and a Quality Specialist from February 2006 to March 2008. Before entering the medical industry, they worked as a Pharmacy Technician at Cub Pharmacy from June 2003 to June 2006 and at Wal Mart Pharmacy from September 2002 to June 2003.

Jessica Montejo has a strong educational background in both business and medical technology. Jessica obtained their Bachelor of Science (B.S.) degree in Medical Technology- Clinical Laboratory Sciences in 2006 from Rosalind Franklin University of Medicine and Science. Following that, they pursued a Master of Business Administration (MBA) degree from Keller Graduate School of Management of DeVry University, completing it in 2009.

In addition to their formal education, Jessica has also obtained additional certifications related to regulatory affairs. In 2013, they received the Regulatory Affairs Certification (US) from RAPS (Regulatory Affairs Professionals Society), as well as the RAC-US (Regulatory Affairs Certification) from the Regulatory Affairs Certification Program.

Overall, Jessica has demonstrated a commitment to both medical technology and regulatory affairs through their education and certifications.