• Coordinated with interdisciplinary study team members to determine best methods to use of laboratory hardware and software systems for desired study results. • Supported clients in the pharmaceutical, medical device, contract research organization and infectious disease fields by using technical expertise to analyze system technical requirements and provides appropriate input to both the development and selection of solutions for laboratory applications.• Work with internal and external validation teams to develop system requirements, as well as identify and document installation and operational qualifications under GLP (Good Laboratory Practices) guide lines. • Detected and documented laboratory systems issues to identify and coordinated proper resources to resolve issues.• Lead multiple development teams to produce application and algorithms under a Software Life Cycle for the GLP environment for research laboratory use. • Member of the Safety Pharmacology Society since inception in 1999 and served on the Outreach Committee. • Awarded funding to initiate a Safety Pharmacology Lecture Series at Texas A&M University