Maria Mccabe
About Maria Mccabe
Maria Mccabe is the QC Technician Lead for Microbiology EM at Bristol-Myers Squibb in New York, with over 20 years of experience in microbiology and quality control.
Current Role at Bristol-Myers Squibb
Maria Mccabe is currently working as a QC Technician Lead for Microbiology EM at Bristol-Myers Squibb in New York, New York. She has been in this role since 2016, where she leads the microbiology environmental monitoring team. Her responsibilities include overseeing quality control processes to ensure compliance with industry standards and regulatory requirements.
Career at Pfizer
Maria Mccabe spent a significant portion of her career at Pfizer, where she worked for a total of 13 years. From 2003 to 2014, she held roles as a QC Microbiology Specialist and Supervisor. Following that, she served as a QC ICC Supervisor from 2014 to 2016. In these positions, she was responsible for maintaining microbiological quality standards and supervising the quality control processes.
Experience at Ipsen and Cruinn Diagnostics Ltd
Before joining Pfizer, Maria Mccabe worked at Ipsen as a Plant Microbiologist from 2000 to 2003. Prior to this, she served as QC and QA Manager at Cruinn Diagnostics Ltd from 1998 to 2000 in Dublin, Ireland. These roles provided her with valuable experience in both quality control and quality assurance, solidifying her expertise in the microbiology field.
Educational Background
Maria Mccabe has a strong academic background in science and technology. She earned a Bachelor of Science degree from the Institute of Technology, Tallaght, studying there from 1995 to 1999. She also holds a Master of Science degree from TU Dublin in Computer Science, completed between 2007 and 2009.
Expertise in Microbiology and Quality Control
With over 20 years of experience in microbiology and quality control, Maria Mccabe has a comprehensive background in the field. She has managed quality control and assurance teams, developed and implemented QC protocols, and ensured compliance with regulatory standards. Her extensive experience spans multiple high-profile roles across leading pharmaceutical companies.