Enoch Reid

Engineer Iii, Validation @Thermo Fisher Scientific

Greenville, NC, US

Responsible primarily for writing Clinical Trial Material Assessments for the Pharmaceutical Development Services (PDS) division of Thermo Fisher Scientific\'s Greenville, NC plant site. Other duties and responsibilities also include writing new testing and sampling protocols and overseeing their subsequent execution as well as validating and qualifying new filling components such as new filters used in the production of PDS drugs. I also train new and existing employees on validation testing techniques as they pertain to validation and the revalidation of existing production and lab sterilizing and depyrogenation equipment relating to steriles drug production. This equipment ranges from steam and terminal sterilizers, manufacturing tanks, pallet tanks, Lev Mixers, depyrogenation tunnels and ovens, and SIP processes for Fillers on filling lines and also some packaging equipment.