Mick Giles
About Mick Giles
Mick Giles is the Senior Director of Quality Operations at Bristol Myers Squibb in Dublin 15, with over 20 years of experience in quality operations and management within the pharmaceutical industry.
Current Role at Bristol Myers Squibb
Mick Giles serves as the Senior Director of Quality Operations at Bristol Myers Squibb, based in Dublin 15. In this role, he oversees quality operations, ensuring compliance with regulatory standards and enhancing the overall quality management system within the organization. His broad experience in the pharmaceutical industry contributes to his leadership in maintaining the highest quality standards.
Previous Experience at Bristol Myers Squibb
Prior to his current role, Mick Giles worked as the Director of Quality Operations for the EMEA and Asia Pacific regions at Bristol Myers Squibb from 2014 to 2021. During his seven-year tenure, he was responsible for managing and improving quality operations across diverse geographical areas, ensuring that all processes adhered to stringent regulatory requirements.
Role at LEO Pharma
Mick Giles held significant roles at LEO Pharma, including a position as the Global Compliance Lead for the SAP project from 2013 to 2014 in Copenhagen, Denmark. In this role, he focused on implementing global compliance strategies within the SAP framework. Additionally, he served as a Quality Assurance Manager from 2011 to 2013 in Dublin, Ireland, where he managed quality assurance processes and ensured regulatory compliance.
Early Career at MSD and Schering Plough
Mick Giles began his career at Schering Plough, where he worked as a QC Manager from 1997 to 2003, managing quality control operations. He then moved to MSD, serving as a Quality Systems Manager from 2003 to 2011. In these roles, he developed a comprehensive understanding of quality systems and quality control processes, laying a strong foundation for his subsequent leadership positions in the industry.
Educational Background in Pharmaceutical Sciences
Mick Giles has an extensive educational background in pharmaceutical sciences. He earned a Bachelor of Science in Analytical Science from Dublin City University, studying from 1991 to 1995. He furthered his expertise with a Post Graduate Diploma in Pharmaceutical Manufacturing Technology from Trinity College, Dublin, which he completed between 2001 and 2002. These qualifications have underpinned his successful career in quality operations and management.