|
Beth Staub was named vice president regulatory affairs and quality assurance in April 2006. Ms. Staub is responsible for overseeing Stryker’s compliance with worldwide product quality and regulatory requirements including FDA and other regulatory bodies.
Ms. Staub began her career with Stryker in April 1989 and held a number of quality regulatory and operational positions within the Company’s Orthopaedics division including manager quality assurance; team leader for the packaging cell; manufacturing team leader for the external support cell; director of the knee steering team; vice president quality assurance regulatory compliance and clinical research; and director of the business process excellence project. She then served as director regulatory affairs and quality assurance for the Company from 2005 to 2006.
Prior to joining Stryker Ms. Staub spent six years with Baxter Healthcare in a variety of quality assurance positions.
Ms. Staub holds a B.S. in Medical Technology from York College of Pennsylvania. | 