Brittany Bell

Background

About Brittany Bell

Brittany Bell (Alston) is the Manufacturing Quality Manager at Kymanox with experience in biopharma, medical device, API pharmaceutical, and sterile compounding operations and compliance. Brittany has expertise in purification process development, process scale up, technology transfer, process validation, investigations, root cause analysis and remediation, CGMP quality and compliance support, auditing and gap assessments, manufacturing quality and batch disposition. Brittany’s technical background and 13+ years of experience is combined with a passion for making quality and science-based decisions with the focus on patient safety to support our clients in maintaining quality systems, and supporting production and quality processes, and delivering quality therapies to our patients. Brittany is a technical subject matter expert in purification process development with technology transfer experience encompassing various expression biologics systems, oral solid dose, API, and compounding pharmacy processes. Brittany’s experience includes the development of a mAb platform purification process from concept to bench scale demonstration, and implementation in the CGMP single-use manufacturing space. Brittany contributes to project success with her technical and quality and compliance expertise, as well as strong leadership and communication skills. Brittany is an ASQ Certified Quality Auditor. She graduated from North Carolina State University with a Bachelor of Science degree in Biological & Agricultural Engineering and pursued graduate level coursework at the Biomanufacturing Training and Education Center, including Upstream, Downstream, and Lyophilization principles.