Lindsey Titus

Lindsey Titus is a Medical Device Quality and Compliance Professional with diverse experience in Post-market Complaint Handling/Vigilance, Design Quality, and Process Engineering. Lindsey's background includes roles in research and production supervision at Alcon Laboratories, where they managed production schedules and led cross-functional improvement teams. At Getinge, Lindsey advanced to roles such as Design Quality Engineering Manager and Sr. Complaint Process Improvement Manager, ensuring compliance with regulatory requirements and overseeing medical device risk management programs. Lindsey holds a Master's degree in Biomedical Engineering from the University of Connecticut and a Bachelor's degree in Biomedical Engineering and International Studies from Worcester Polytechnic Institute.