Ken Shannon
About Ken Shannon
Ken Shannon is a Commissioning, Qualification, and Validation Engineer at Bristol-Myers Squibb in New York with over a decade of experience in the pharmaceutical industry.
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Ken Shannon is currently a Commissioning, Qualification, and Validation Engineer at Bristol-Myers Squibb in New York, New York, United States.
Current Company: Bristol-Myers Squibb
Ken Shannon has been with Bristol-Myers Squibb for over 7 years, where he serves as a Commissioning, Qualification, and Validation Engineer. His role involves ensuring that systems and processes meet regulatory and performance standards within their pharmaceutical operations.
Past Experience: Alexion Pharmaceuticals, Inc.
Before joining Bristol-Myers Squibb, Ken Shannon worked as a Process Engineer at Alexion Pharmaceuticals, Inc. from 2015 to 2016. During his year-long tenure, he was responsible for various engineering processes within the company.
Previous Roles at MSD
Ken Shannon has substantial experience with MSD, having worked there as a Process Engineer from 2013 to 2015, following a 5-month internship in 2012. His roles at MSD contributed significantly to his expertise in process engineering.
Education and Academic Background
Ken Shannon holds a Master of Science (2016-2018) and a Bachelor of Science (2009-2013) from Dublin City University. His academic journey provided a solid foundation in science and engineering, which underpins his capabilities in the pharmaceutical industry.
Experience in the Pharmaceutical Industry
With over a decade of experience in the pharmaceutical industry, Ken Shannon has a strong background in process engineering and validation. His roles have spanned both the United States and Ireland, showcasing his flexibility and expertise in various engineering functions within the industry.