Ingrid Caton
About Ingrid Caton
Ingrid Caton is a Lead Project Manager at Mammoth Biosciences with extensive experience in project management across various organizations, including Bio-Rad Laboratories and Viracor - Eurofins. She specializes in managing projects in regulated environments and has a strong background in developing and monitoring project plans and budgets.
Current Role at Mammoth Biosciences
Ingrid Caton serves as the Lead Project Manager at Mammoth Biosciences, a position she has held since 2022. In this role, she is responsible for overseeing project management activities, ensuring that projects align with the company's strategic goals. Her expertise in managing projects in regulated environments supports the development of innovative solutions in the biotechnology sector.
Previous Experience at Mammoth Biosciences
Prior to her current role, Ingrid worked as a Senior Project Manager at Mammoth Biosciences from 2021 to 2022. During this tenure, she contributed to various projects, leveraging her extensive background in project management to drive successful outcomes in a fast-paced environment.
Experience at Bio-Rad Laboratories
Ingrid Caton held multiple positions at Bio-Rad Laboratories, including Bio-Rad Project Manager III from 2019 to 2021 and Project Manager II from 2017 to 2019. Her responsibilities included managing project plans, schedules, and budgets, as well as ensuring compliance with industry standards in the development of medical devices and clinical diagnostics.
Educational Background
Ingrid Caton has a strong academic background, having studied at multiple institutions. She achieved a Doctoral Candidate status in Business Administration and Management from Northcentral University, where she studied from 2014 to 2022. Additionally, she earned a Master's degree in Biology from Wichita State University between 2003 and 2007 and a Bachelor of Science in Industrial Microbiology from Pontificia Universidad Javeriana from 1996 to 2002.
Specializations and Skills
Ingrid specializes in facilitating cross-functional relationships across various workstreams and communication channels. She has extensive experience in managing projects in regulated environments, including FDA, ISO, MDSAP, and GMP standards. Her expertise encompasses program and portfolio management for medical devices, clinical diagnostics, and biopharmaceutical services, along with a proven track record in leading new product development and technology transfer initiatives.