Manager, Site Quality Systems, Curia
Kristin Shuler is an industry professional in the areas of Quality Assurance, Compliance, Validation, and Engineering. She has experienced the gambit of pharmaceutical development from clinical and commercial API, Finished Pharmaceuticals, and OTC Production. Her team is responsible for oversight of the QMS at the Curia Wisconsin site including deviations, CAPA, training, validation, internal/external audits, environmental monitoring, annual product reports, onboarding of computerized systems and quality programs, and site/corporate metrics. Her broad base of knowledge allows her to take a practical and “bigger picture” approach to validation and quality activities. She is currently at work creating guidelines for her site on application of QMS and GxP topics for clinical phase materials.