Wil Cainglet has extensive experience in the field of quality assurance and document control. Wil is currently working as a Document Control Manager (QA) at Eidos Therapeutics since January 2022. Prior to this, they held the position of Document Control Specialist (QA) at the same company from February 2020 to January 2022.
Before joining Eidos Therapeutics, Wil worked as a Quality Assurance Specialist at Tecan Genomics, Inc. from November 2018 to December 2019. Wil also served as a QA Document Control Specialist at Gritstone Oncology from June 2018 to November 2018.
In 2017, Wil worked at Genentech as a QA Product Technical Manager / IMP Quality Systems & Compliance from May 2017 to April 2018. Prior to that, they gained experience at Gilead Sciences as a QA Inspector III / Distribution Specialist IV from May 2012 to April 2017.
Wil's career in the pharmaceutical industry began at BioMarin Pharmaceutical Inc. where they worked as a Quality Assurance / Quality Control Specialist from June 2008 to June 2012. Wil also briefly worked at Tissue Bank International, Inc. as a Quality Control Laboratory Technician for the month of June 2008.
Before entering the pharmaceutical industry, Wil worked as a Quality Control Laboratory Technician at National Food Laboratory, Inc. from May 2004 to August 2004. Wil also gained internship experience at Chiron Corporation as a QC Microbiology Intern in both 2003 and 2002.
Wil Cainglet attended San Francisco State University from 2004 to 2008, where they obtained a Bachelor of Arts (B.A.) degree in Psychology.
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