Mark Casey
About Mark Casey
Mark Casey is the Manager of Quality Operations, QP Team at Bristol Myers Squibb, with over 20 years of experience in the Pharma, Biopharma, and Medical Devices industries.
Current Roles at Bristol Myers Squibb
Mark Casey currently holds two key positions at Bristol Myers Squibb. He is the Manager of Quality Operations for the QP Team and also serves as the Manager of Regulatory Compliance. In these roles, he is responsible for ensuring the quality and safety of biopharmaceutical products. His work likely involves collaboration with cross-functional teams to address quality issues and ensure compliance with industry standards in Dublin, County Dublin, Ireland.
Previous Experience at Bristol Myers Squibb
Before his current roles, Mark Casey was a Senior Regulatory Compliance Specialist at Bristol Myers Squibb from 2019 to 2020. During his tenure, he was involved in maintaining regulatory compliance and possibly risk management strategies for one year. His experience in regulatory compliance has been integral to his career progression within the company.
Career at DCC Vital
Mark Casey served as a Senior Regulatory Affairs Technical Consultant/Officer at DCC Vital from 2015 to 2019. Over the course of four years, he was involved in regulatory affairs, contributing to the company's compliance with industry regulations and standards in Dublin.
Academic Background
Mark Casey has a strong academic background, beginning with a BSc in Biotechnology from the National University of Ireland, Maynooth, where he studied from 1997 to 2001. He further honed his skills through a Management Training Course in 2018 at Pro Populus and an Auditing Course in 2016 at The Compliance Group. This educational foundation has equipped him with the knowledge and expertise to excel in his various roles in the pharmaceutical and medical devices industries.
Early Career and Various Roles
Mark Casey's career spans over 20 years in the Pharma, Biopharma, and Medical Devices industries. He has held numerous roles, including Quality Engineer at Nypro, a Jabil Company, and QA Operations Specialist at Pfizer. Additionally, he worked as a Validation Engineer at BD Medical and a Business Manager for Tech Transfer at BSP Pharmaceuticals. His diverse experience has provided him with a wide range of skills in areas including Lab, Validation, Quality, Project Management, and Regulatory Affairs.