Colleen Turner
About Colleen Turner
Colleen Turner is the Director of IT Validation Services at Bristol-Myers Squibb in New York, with over 25 years of experience in IT validation and quality assurance.
Current Position at Bristol-Myers Squibb
Colleen Turner currently serves as the Director of IT Validation Services at Bristol-Myers Squibb. Based in New York, New York, United States, she plays a critical role in overseeing IT validation initiatives within the company. Her work ensures that IT systems used in various processes adhere to stringent industry standards and regulatory requirements.
Previous Roles at Bristol-Myers Squibb
Colleen Turner has held multiple key positions at Bristol-Myers Squibb over the last two decades. From 2006 to 2011, she was the Director of R and D Informatics Quality and Compliance, where she focused on ensuring compliance with research and development informatics. Prior to that, she served as Associate Director of Informatics Quality Assurance from 2003 to 2006, and as a Quality Assurance Advisor from 2000 to 2003.
Experience at Taratec Corp and Huntingdon Life Sciences
Colleen Turner worked at Taratec Corp before joining Bristol-Myers Squibb, holding positions such as Principal Validation Consultant, Senior Validation Consultant, and Validation Consultant between 1996 and 2000. Earlier in her career, she was with Huntingdon Life Sciences, where she served as Manager of IT Services from 1994 to 1996 and as Computer Systems Coordinator from 1988 to 1994.
Educational Background
Colleen Turner's academic credentials include a Master of Science degree from Temple University and a Bachelor of Science degree from Rutgers University (Cook College). Her educational background has equipped her with the necessary skills and knowledge to excel in IT validation and quality assurance.
Expertise in IT Validation and Quality Assurance
With over 25 years of experience, Colleen Turner is a seasoned professional in IT validation and quality assurance. She has extensive experience managing IT services and compliance in the pharmaceutical industry. Throughout her career, she has successfully led multiple IT validation projects, ensuring adherence to regulatory standards in highly regulated environments.