Carolyn Devlin
About Carolyn Devlin
Carolyn Devlin is the QA Document Management Lead at Bristol Myers Squibb in Ireland, with extensive experience in QA Systems and a strong background in Chemistry and Biopharma.
Title
Carolyn Devlin is the QA Document Management Lead at Bristol Myers Squibb in Ireland.
Current Role at Bristol Myers Squibb
Carolyn Devlin currently holds the position of QA Document Management Lead at Bristol Myers Squibb in Ireland. In this role, she oversees the document management processes within the QA department, ensuring quality control and compliance with industry standards.
Past Roles at Bristol Myers Squibb
Before her current role, Carolyn Devlin served in several positions at Bristol Myers Squibb. She was a QA Systems Specialist from 2019 to 2021 in County Dublin, Ireland. Prior to that, she worked as a QA Associate from 2017 to 2019 and as a Quality Systems Documentation Coordinator from 2016 to 2017, both at the Cruiserath Biologics site in Co. Dublin. Her career at BMS began as a QA Systems Intern in 2016 for 5 months, also at Cruiserath Biologics.
Role at Royal Society of Chemistry
Carolyn Devlin worked as a Publishing Editor at the Royal Society of Chemistry from 2014 to 2015 in Cambridge, United Kingdom. In this role, she was involved in the management of scientific publications, contributing to the dissemination of chemical research.
Education and Professional Training
Carolyn Devlin achieved a Doctor of Philosophy (Ph.D.) in Chemistry from Queen's University Belfast, where she studied from 2009 to 2013. Before her Ph.D., she earned a Master's Degree in Chemistry from the same university, studying from 2005 to 2009. In 2016, she enhanced her expertise in the biopharmaceutical field by completing a Certificate in Quality Analytics for Biopharma at Nibrt/ITSligo.
Skills and Special Interests
Carolyn Devlin is skilled in managing Quality Systems, including Document Management, Record Retention, Change Control, Quality Risk Management, Internal Auditing, Training Development & Delivery (including GMP), and Technical Writing. She has a special interest in Quality Culture development and Diversity & Inclusion in the workplace. Her expertise is backed by extensive experience in the biopharmaceutical industry, particularly in QA Systems.