Caitlin Ambrose
About Caitlin Ambrose
Caitlin Ambrose is a Technical Writer at Bristol Myers Squibb with a diverse background in quality control, cell processing, and quality assurance.
Current Role as Technical Writer
Caitlin Ambrose is currently a Technical Writer at Bristol Myers Squibb in Summit, New Jersey. She began this role in January 2020. Her responsibilities likely include creating and managing technical documentation, working to ensure clarity, accuracy, and compliance with industry standards.
Position at Celgene
Caitlin Ambrose also holds a concurrent position as a Quality Control Associate at Celgene in Warren, New Jersey. In this role, she is responsible for maintaining quality standards, conducting inspections, and ensuring compliance with regulatory requirements.
Previous Experience at Novartis
Caitlin Ambrose worked at Novartis as a Cell Processing Specialist. During her 9-month tenure from 2017 to 2018 in Morris Plains, New Jersey, she was involved in the processing and handling of cellular products, contributing to the company's biotechnological operations.
Quality Assurance Role at Immunomedics
Before joining Novartis, Caitlin Ambrose worked at Immunomedics as a Quality Assurance Associate. From 2015 to 2017, she spent two years focusing on ensuring the quality and regulatory compliance of biopharmaceutical products.
Educational Background in Biology
Caitlin Ambrose earned her Bachelor of Science (B.S.) degree in Biology, General from Fairleigh Dickinson University-Florham Campus, where she studied from 2011 to 2015. Her academic background in biology underpins her professional work in various scientific and technical roles.
Teaching Assistant at Fairleigh Dickinson University
In 2013, Caitlin Ambrose served as a Teaching Assistant at Fairleigh Dickinson University. She assisted in the course 'Intro to Molecules, Cells, & Genes,' contributing to the academic development of students in the field of molecular biology.