Audrey Whitford
About Audrey Whitford
Audrey Whitford is the Senior Manager, Global Quality Serialization and Product Surety at Bristol Myers Squibb, with extensive experience in quality assurance and regulatory affairs across multiple regions.
Current Title
Audrey Whitford is currently serving as the Senior Manager, Global Quality Serialization and Product Surety at Bristol Myers Squibb. She oversees global initiatives ensuring the quality and security of the company's products.
Work Experience at Bristol Myers Squibb
Audrey Whitford has held multiple positions at Bristol Myers Squibb, showcasing her growth within the company. Starting as a Senior Quality Operations Specialist from 2015 to 2020 in Dublin, she was promoted to Manager, Quality Operations, Drug Product, EMEA and Asia Pacific, roles she held for two months in 2020-2021. She currently holds the position of Senior Manager, Global Quality Serialization and Product Surety.
Education Background
Audrey Whitford's academic qualifications include an M.Sc. in Pharmaceutical Technology and Quality Systems from University College Cork (2017-2019) and an M.Sc. in Pharmaceutical QA & Regulation from Dublin Institute of Technology (2013-2015). Additionally, she achieved a B.Sc. (Hons) in Food/Pharmaceutical Science from Dublin Institute of Technology (2004-2008).
Early Career and International Experience
Audrey Whitford's career began with roles such as QA/QC Analyst at Ricesteele Manufacturing Ltd (2008-2009) and QA Supervisor / HACCP Coordinator at New Food Classics in Canada (2009). She gained further experience in quality assurance and regulatory affairs at United Drug from 2010 to 2014 and at Servier from 2014 to 2015.
Expertise in Quality Assurance and Regulatory Affairs
Audrey Whitford has a comprehensive background in quality assurance and regulatory affairs, leading initiatives across various regions including EMEA and Asia Pacific. Her diverse experience includes roles in both food and pharmaceutical industries, from ensuring compliance and product safety to managing regulatory constraints.