Brian has over six years of experience in contamination control, environmental monitoring, and risk-reduction systems. He provides application reviews, assists with the application and requirements of ISO standards related to manufacturing, conducts site walk-downs to review and troubleshoot solutions, and consults on the implementation of real-time monitoring systems. Brian is experienced in both viable and non-viable sampling, as well as sampling of liquids in ultrapure water (UPW), water for injection (WFI), and deionized (DI) water systems. His services support a range of industries, including pharmaceutical, semiconductor, aerospace, automotive, medical device, compounding pharmacy, healthcare, and battery manufacturing.
In addition, Brian brings more than 20 years of expertise in the application of containment systems for the pharmaceutical, chemical, and biotech sectors. His background includes conducting application reviews, delivering on-site presentations and training, and developing custom designs for handling potent compounds. His application experience spans from bench-top research through scale-up and into full manufacturing. Brian’s proficiencies include the safe handling of active pharmaceutical ingredients (APIs), developing containment strategies aligned with occupational exposure limits (OELs) and banding practices, and providing solutions for formulation and current Good Manufacturing Practice (cGMP) applications. His specialties include OEB 3 & 4, potent compound weighing and handling, and user protocol development.
