Louise Keane

Louise Keane is currently serving as the Regulatory Affairs Manager for Neurosurgical at Stryker since February 2022. Previously, Louise worked as a Sterilization Engineer at Abbott, providing technical support for sterilization processes and managing requalification projects. Prior experience includes a role as Senior Quality Engineer at Sanmina (Medical Devices), where responsibilities encompassed audit preparation, technical documentation, process validation, and quality issue resolution. Earlier career roles included Quality Technician at Sanmina, Clinical Trials Researcher at University Hospital Limerick/NUI Galway, and multiple management positions in food and beverage operations. Louise holds a PG Diploma in Entrepreneurship from Trinity College Dublin, a Bachelor's Degree in Science and Technology from NUI Galway, and is currently pursuing a Master's degree in Pharmaceutical Regulatory Affairs at the Institute of Technology, Carlow.