Director of Quality Assurance
Bringing over 15 years of Quality experience in roles of ascending responsibility in both Quality Assurance and Quality Systems.
She began her career in vaccine manufacturing in the biopharmaceutical industry including roles in quality assurance and quality systems spearheading deviation, CAPA, and change controls as subject matter expert for all quality assurance including internal and external audits. Her Quality Systems experience included hosting regulatory audits including stateside (US FDA) and other global agencies (European Union (EU), United Kingdom (MHRA) and other Mutual Recognition Agreement countries).
Melissa has the responsible for Quality Assurance oversight of all aspects of our Manufacturing operations, from new product development to commercial batch release. She leads a team of associates and specialists responsible for the quality and compliance requirements throughout batch manufacturing, batch release, deviation, change control, and validation activities at Bryllan.