Brendan Garrett
About Brendan Garrett
Brendan Garrett is a CSV Specialist at Bristol Myers Squibb in Dublin, Ireland, with over 20 years of experience in the pharmaceutical and medical device industries.
Current Position at Bristol Myers Squibb
Brendan Garrett currently holds the position of CSV Specialist at Bristol Myers Squibb, based in Dublin, County Dublin, Ireland. His responsibilities likely include overseeing computer system validations to ensure compliance with regulatory standards. His role ensures that electronic systems within the company are validated according to industry standards.
Previous Experience in CSV and Automation
Brendan Garrett has accumulated extensive experience in various roles over his career. He worked as an Automation Engineer at MSD in Carlow, Ireland, from 2020 to 2021. Additionally, he served as a CSV Engineer at Takeda in Dunboyne from 2019 to 2020 and at Bristol-Myers Squibb from 2017 to 2019. His roles in these positions involved ensuring that automated systems were validated and compliant with standards.
Early Career in Laboratory and Quality Assurance
Brendan Garrett's early career includes roles in laboratory and quality assurance settings. He worked as a QA Analyst at VistaMed and Laboratory Chemist at Baxter International Inc. He also served as a Data Integrity Analyst at Pfizer for six months in Grange Castle in 2017. These positions involved maintaining the quality and integrity of laboratory data and systems.
Educational Background in Pharmaceutical Sciences
Brendan Garrett achieved a Bachelor's degree in Pharmaceutical Sciences from the Institute of Technology, Sligo, where he studied from 2002 to 2006. This educational background laid the foundation for his extensive career in the pharmaceutical and medical device industries. His studies provided him with the technical knowledge necessary for his various roles.
Decade-Long Tenure at Takeda Pharmaceuticals
One of Brendan Garrett's significant career milestones is his decade-long tenure at Takeda Pharmaceuticals, where he served as a QC LIMS Administrator from 2007 to 2017. During this period, he was responsible for managing laboratory information management systems and ensuring quality control processes were up to standard. His long-term commitment to this role highlights his expertise and reliability in the field.