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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.
Elizabeth brings to this position, a strong background for the role, having spent 15 years in the Pharmaceutical and Medical Device sectors with Boston Scientific, Medtronic, Baxter and Allergan Pharmaceuticals prior to joining Nelipak in September of 2012 as Quality & Continuous Improvement Manager of the groups Irish facility.
As Nelipak Healthcare Packaging’ Director of Global Quality & Regulatory Affairs, Elizabeth will lead the Quality team in developing and delivering Quality Management Strategies and Quality Operational Excellence Programs across Nelipak’s manufacturing sites. Elizabeth will manage the Groups Quality Certification programs proactively promoting Nelipak’s Quality systems and improvements at Key Accounts.
“The quality of dedication and customer satisfaction is important to Nelipak’s long-term success. We look forward to Elizabeth’s continued contribution to the future growth of the organisation in her new role.”
