Claire O' Neill
About Claire O' Neill
Claire O' Neill is a Manufacturing Support Scientist/Engineer at Bristol Myers Squibb with extensive experience in downstream processing within a GMP environment.
Current Title and Role
Claire O'Neill holds the position of Manufacturing Support Scientist/Engineer at Bristol Myers Squibb. She started this role in July 2020. Her responsibilities likely involve supporting manufacturing processes to ensure compliance with industry standards and regulations.
Professional Experience at Bristol Myers Squibb
Prior to her current position, Claire worked as a Bioprocess Associate at Bristol Myers Squibb for three years from 2017 to 2020. In this role, she would have gained significant experience in biopharmaceutical processes, contributing to product development and manufacturing.
Professional Experience at Pfizer
Before joining Bristol Myers Squibb, Claire worked at Pfizer in Grange Castle. She served as a Process Technician from 2015 to 2017, and prior to that, as a Visual Inspection Operative from 2014 to 2015. These roles involved ensuring quality control and adherence to Good Manufacturing Practices (GMP) in pharmaceutical production.
Educational Background
Claire O'Neill has a robust educational background in bioprocessing and related fields. She earned a Master's degree in Bioprocess Engineering from Dublin City University (2020-2022). Additionally, she holds a Certificate (Level 8) in Bioprocessing from the Institute of Technology, Tralee (2018-2019), a Bachelor of Science (BSc) in Forensic Toxicology from Athlone Institute of Technology (2013-2014), and completed three years of study in Chemistry and Biochemistry at University College Dublin (2009-2012).
Early Career and Work Experience
Claire's career began with a one-month work experience in the Biochemistry Lab at St. James's Hospital in 2014. This initial exposure provided her with practical insights into the field of biochemistry, which have been foundational to her subsequent roles in the biopharmaceutical industry. Her early experiences have contributed to her strong professional background in the industry.
Expertise in Downstream Processing
Claire O'Neill has extensive experience in downstream processing within a Good Manufacturing Practice environment. This expertise involves various stages of biopharmaceutical production, including purification and quality assurance, ensuring that the final product meets regulatory standards.