Mick Keating
About Mick Keating
Mick Keating is a QC Analyst at Bristol-Myers Squibb in Cruiserath with a strong background in quality assurance and regulatory affairs.
Title
Mick Keating currently holds the position of QC Analyst at Bristol-Myers Squibb, where he is involved in quality control processes at the Cruiserath facility.
Current Role at Bristol-Myers Squibb
As a QC Analyst at Bristol-Myers Squibb in Cruiserath, Mick Keating focuses on maintaining high-quality standards in pharmaceutical production. His role includes conducting various analytical tests and ensuring compliance with industry regulations. He employs techniques such as High Performance Liquid Chromatography and Capillary Electrophoresis in his daily tasks.
Former Positions at Bristol-Myers Squibb
Mick Keating previously served as a QA Associate - Batch Certification at Bristol-Myers Squibb in County Dublin from 2017 to 2019. He was responsible for the certification of drug product batches. Before that, he worked as a Quality Systems and Compliance Intern in 2016, where he contributed to the maintenance of quality systems and compliance protocols.
Education and Academic Achievements
Mick Keating earned a Master of Science in Pharmaceutical Regulatory Affairs from the Institute of Technology, Carlow, from 2020 to 2021, graduating with First Class Honors. His academic focus included Gene Therapy (ATMP), Quality Risk Management, Pharmacovigilance, and Pharmaceutical Quality Systems. He also holds a degree in Biotechnology from Dublin City University, where he studied from 2013 to 2017.
Technical Skills and Expertise
Mick Keating has expertise in several analytical techniques and quality assurance processes. His technical skills include High Performance Liquid Chromatography, Capillary Electrophoresis, Karl Fischer Titration, SDS-PAGE, and use of tools such as Delta V and PI Vision. His professional focus is on Drug Product Batch Release.