Lisa M.

Lisa M. has over 20 years of work experience in regulatory affairs and quality assurance roles. Lisa is currently working as the Director of Regulatory Affairs and Quality Assurance at Vertos Medical Inc, a position they have held since April 2018. Prior to this, they were the Director of Regulatory Affairs and Quality Assurance at ReShape Medical, Inc. from August 2017 to March 2018. Lisa has also worked as a Senior Manager of Regulatory Affairs at ReVision Optics from January to July 2017, and as a Senior Regulatory Affairs Manager at Glidewell Dental Lab from March 2016 to January 2017. Before that, they held the position of Principal Regulatory Affairs Specialist at TriVascular, Inc. from July 2014 to March 2016. Lisa has also worked as a Senior Regulatory Affairs Specialist at Insightra Medical Inc from September 2013 to July 2014, and at Neomend from December 2007 to September 2013. Lisa started their career as a Documentation Manager at Alsius Corporation from January 2002 to April 2004, and later worked as a QA/Documentation Manager at Premier Laser Systems, Inc. from September 1996 to December 2000.

Lisa M. obtained a Bachelor of Arts degree in Law and Society from UC Santa Barbara. In June 2019, they also obtained a certification in RAC-US from the Regulatory Affairs Certification Program. Additionally, in November 2016, they became a member of the Regulatory Affairs Professionals Society (RAPS). Currently, Lisa M. is attending Northwestern University - Kellogg School of Management, but the specific degree and field of study are not provided.