To strengthen our commitment to delivering unparalleled expertise and support to the medical device and pharmaceutical markets several new positions that take on a global scope are being created.
The first of these positions is the appointment of Elizabeth Nugent to the role of Director of Global Quality & Regulatory Affairs.
Elizabeth received her Bachelors of Science and Masters of Business Administration (MBA) from the University of Limerick. She is a certified Six Sigma Black Belt, Process and Product Validation Subject Matter Expert and experienced in ISO 13485 & FDA Regulations. In addition she has over 10 years of manufacturing experience in Quality and Process Engineering / Management roles.