Nicole Sandoval

Director, Quality Management System at AlterG

Nicole Sandoval has over 29 years of work experience in various companies and roles. From 1992 to 1996, they worked as a CAD Drafter Detailer at MedaSonics, where they were responsible for detailing production parts and implementing engineering change orders. Nicole then joined ADAC Laboratories as a Sr. Designer Drafter from 1996 to 2001.

In 2001, they started working at Philips Healthcare as an Engineering Services Supervisor. During their tenure, they managed the workload of drafters and designers, supported work requests from various departments, and completed drafting requests and new design documentation. Nicole held this position until 2012.

From 2012 to 2013, they worked as a Document Control Specialist at Velodyne Lidar, Inc. Nicole then joined Varian Medical Systems as a Mechanical Designer V from 2013 to 2014.

In 2014, they joined Thermofisher Scientific as a Designer for a year before joining AlterG in 2015. At AlterG, they initially worked as a QA Change Analyst until 2018. Nicole was then promoted to Manager, Quality & Doc. Control, where they managed quality assurance objectives and international documentation for government bodies. Currently, they hold the role of Director, Quality Management System at AlterG.

Nicole Sandoval's education history includes several academic achievements and certifications. From 2009 to 2011, they attended Ashford University, where they obtained a Bachelor of Arts degree in Organizational Management. Prior to that, in 2009, they earned a Wildfire 4.0 Certificate in Intro to ProEngineer from Nx Rev. In 1997, they obtained a SolidWorks Certification from GEI Technology. Additionally, they attended Masters Institute from 1991 to 1993, where they earned an Associate of Science degree in Electrical & Mechanical Design Drafting. There is no specific information regarding their education at Central County Occupational Center in 1990.

Furthermore, in 2022, Nicole Sandoval obtained a Regulatory Affairs Certificate in Medical Devices from the Regulatory Affairs Certification Program.

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