Validant
Chrys Kyee is a Senior Project Manager at Validant since December 2020, previously serving as a Senior Business Analyst and Project Lead at Genentech from February 2001 to December 2020. At Genentech, Chrys led significant projects that resulted in the implementation of TrackWise Global Change Control across over 20 sites in both Biologics and Small Molecules Operational Units. Mentorship was provided to a junior team member in maintaining and enhancing support processes using the SCRUM methodology. Chrys also spearheaded changes in the Global Product Complaint System, improving On Time Closures, and implemented a new mechanism for GMP system account provisioning, enhancing operational efficiency. Collaborating with Informatics, Chrys helped institute an agile development methodology, facilitating more effective software changes.
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Validant
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Validant is a full-service life science consulting firm serving developers and manufacturers of pharmaceuticals, biologics, medical devices, and diagnostics worldwide. We partner with these companies to ensure safe and reliable access to life-saving healthcare products, facilitating their efficient, compliant progression from preclinical and clinical phases through to manufacturing and distribution—and optimizing quality at each step. Our platform brings together leading specialists in each facet of the product lifecycle, and we have curated an extensive and diverse global network of consultants to help execute strategies worldwide. Because of this, Validant is able to deliver our breadth of consulting, execution, and support services in the right place, at the right level, and in the right combination to meet your exact need. We've empowered hundreds of clients – from start-ups to the largest global leaders – to efficiently navigate regulatory, compliance, and quality complexities. How can we help you?