Provide quality support of day-to-day quality operations of all elements of the Quality Management System in a cGMP compliant pharmaceutical and medical device laboratory environment.Including:-Operation and administration of QMS (OOS, OOT, CAPA's, change control, supplier controls, sample receipt processes, equipment controls, quality improvement, document and record control, laboratory proficiency testing, training and quality monitoring)- Responsible for ensuring compliance with FDA 21 CFR 820,210 and 211 and ISO 17025- Support quality control with projects, proposals and reports, including reviewing documents and data for good documentation practices- Archiving projects/studies to comply with regulations-Provide training to operations staff in the areas of Quality systems and regulatory compliance

I perform physical testing on plastics, rubber and rubber-like materials. I also assist with quality control and calibrations at our Akron location.

I helped with exhibits, events, and educating on the different species.