Jesse Beckman

Jesse Beckman has a diverse work experience in the field of quality assurance and manufacturing. They started their career as an Undergraduate Research Assistant at Colorado State University from 2009 to 2012. In 2013, they worked as a Manufacturing Associate II at Amgen for a short period. From 2014 to 2016, Jesse worked at Green Mountain Pharmaceuticals, initially as a Manufacturing Associate, then as a Manufacturing Lead, and later as a Quality Assurance Manager. Their responsibilities included managing facility schedules, maintenance, calibration programs, and production records. They also performed manufacturing batch record review and managed deviations, CAPAs, and change controls.

From 2015 to 2016, Jesse also worked as a Project Manager at Belmar Research, where they provided clinical trial drug manufacturing services and developed protocols and processes for the production of clinical trial drugs.

Since 2016, Jesse has been working at KBI Biopharma. They started as a Senior Quality Assurance Specialist, Disposition, where they served as the primary Disposition system manager and led daily disposition status meetings with site leadership. From 2021 to 2023, Jesse held the position of Senior Quality Assurance Manager, providing overall direction to the QA Manufacturing group and managing departmental staffing needs. Currently, Jesse holds the role of Associate Director Quality Assurance at KBI Biopharma.

Overall, Jesse Beckman's work experience showcases their expertise in quality assurance, manufacturing, and project management in the pharmaceutical industry.

Jesse Beckman holds a Bachelor of Science (B.S.) degree in Biomedical Sciences with a minor in Biomedical Engineering from Colorado State University.