Quality Assurance Consultant, BioPoint
Adrienne Leyland is a Quality Assurance professional with 15 years of experience within regulated industries. She has worked in pharmaceutical biologics, QC laboratory settings within the food sector and most recently an FDA-registered 503B Compounding facility. Her specialties within the field include regulatory remediation, developing professional, positive and transparent relationships with regulatory bodies, conducting supplier qualifications and agreements as well as creating and implementing Quality Management Systems from the ground up. She has extensive experience in conducting thorough investigations, developing appropriate and effective CAPA plans, auditing, developing effective standard operating procedures and devising product stability programs. She has presented at multiple conferences, both independently and at roundtable sessions, on the subject of supplier qualifications and how to ensure an organization is cross-functionally aligned with their choice of suppliers. Adrienne’s passion is remediating regulatory issues, fostering a culture of Quality within an organization, collaborating with teams on how to develop the most robust CAPA plans, emphasizing the importance of Quality within a company and teaching others about the diverse, ever-changing and FUN world of a Quality professional.