I've supported pharmaceutical laboratory systems at FAREVA, formerly Pfizer and Wyeth Pharmaceuticals, since 2007. As a Site System Administrator and LabWare LIMS Systems Analyst, I configure, validate, troubleshoot, and support LabWare LIMS in GMP-regulated Quality Control environments.
I helped migrate SQL*LIMS to LabWare LIMS and partner with laboratory stakeholders, validation teams, and IT to translate workflows into system solutions. My work includes master data governance, specifications, test methods, calculations, workflow design, interface testing with Empower and laboratory instruments, and IQ/OQ/PQ execution.
Earlier, I performed raw-material analytical testing at Wyeth using HPLC and GC while following USP, NF, FCC, and internal procedures. I also train users, develop documentation, and maintain data integrity and FDA compliance across laboratory information-management processes.
