Kara Cyr Email & Phone Number

A skilled professional in quality, regulatory compliance, and operations. I excel in developing and optimizing Quality Management Systems (QMS), managing cross-functional teams, and ensuring compliance with FDA, ISO, and other regulatory standards.I am passionate about improving manufacturing processes, mitigating risks, and leading continuous improvement initiatives to enhance product quality and operational efficiency. My expertise includes process validation, supplier management, CAPA, internal audits, and product launch readiness.As Director of Quality Control and Assurance at Vesta Biotherapeutics, I lead the development of robust quality systems and ensure regulatory compliance across all stages of the product lifecycle, from design to production. My goal is to foster a culture of quality, reduce regulatory risks, and deliver high-quality products to market efficiently.Industries: Medical Device Manufacturing | Pharmaceutical Manufacturing

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  Eastern Connecticut State University

  General