ISO 13485 Registered


Gary Seeger

Vice President of Quality Assurance and Regulatory Affairs

Gary Seeger directs the Quality Assurance, Regulatory Affairs and Document Control activities of Stellartech Research Corporation.  Gary has more than 45 years of experience in pharmaceutical and medical device quality assurance and regulatory affairs, including the establishment of  quality systems and the determination of strategic regulatory pathways for medical device clearances and approvals. Gary’s quality system expertise includes QSR, MDD, and ISO 13485 compliance and his regulatory expertise encompasses 510k clearances, IDE, PMA and CE approvals.

Prior to joining Stellartech in 1995, Gary gained medical device experience at companies such as Abbot Laboratories, Allergan Pharmaceuticals, W.L. Gore, EP Technologies and Synvasive.  Gary’s experience encompasses therapeutic energy delivery systems (RF generators and catheters), implants, manual and powered orthopedic equipment, and ophthalmic products. Gary held the position the Vice President of Quality Assurance and Regulatory Affairs at Stellartech Research Corporation from 1995 through 2007, when he left to pursue another opportunity in the medical device field.  Gary rejoined Stellartech in August, 2014. 

Gary is a Certified Quality Engineer (CQE) and Certified Reliability Engineer (CRE) with the American Society for Quality.  Gary holds a BS in Physics from Harvey Mudd College and an MBA from UCLA and served as a Captain and Naval Aviator in the United States Marine Corps.

Gary Seeger