Mark Rogers Ctbs
About Mark Rogers Ctbs
Mark Rogers is a Senior Director of Quality Technical Services at Adaptimmune, with extensive experience in quality assurance and regulatory affairs across various biotechnology companies. He has contributed to significant projects, including the first FDA Investigational New Drug application for Plantar Fasciitis.
Work at Adaptimmune
Mark Rogers currently serves as the Senior Director of Quality Technical Services at Adaptimmune. He has held this position since 2021, contributing to the company's focus on innovative therapies in the field of cell and gene therapy. His role involves overseeing quality assurance and technical services, ensuring compliance with regulatory standards and facilitating the development of high-quality therapeutic products.
Previous Experience in Quality Assurance and Technical Services
Prior to his current role, Mark Rogers accumulated extensive experience in quality assurance and technical services across various organizations. He worked at MiMedx as Vice President of Quality Assurance and Regulatory Affairs from 2015 to 2021. Before that, he held positions at Pioneer Surgical Technology, ImClone Systems, and Bayer Pharmaceuticals, where he focused on validation services and quality control processes.
Education and Expertise
Mark Rogers holds a Bachelor of Science in Chemistry from North Carolina State University, where he studied from 1985 to 1990. He also pursued a Pre-MBA in Business Administration and Management at Furman University from 1990 to 1992. Additionally, he earned an MBA in Value Driven Leadership and Strategy from UNC Kenan-Flagler Business School in 2001. His educational background supports his expertise in quality assurance, regulatory affairs, and product development.
Significant Contributions to FDA Submissions
Mark Rogers authored the Chemistry, Manufacturing, and Controls section of an FDA Investigational New Drug application for Plantar Fasciitis. This submission marked the first-ever IND for this drug indication, highlighting his role in advancing therapeutic development and regulatory compliance in the pharmaceutical industry.
Career Progression and Key Roles
Mark Rogers has a diverse career trajectory, having held various key roles in the pharmaceutical and biotechnology sectors. His previous positions include Technical Services Manager at National Cabinet Lock, Director of Validation and Technical Services at Biomimetic Therapeutics, and Associate Director at Pfizer and ImClone Systems. His experience spans over three decades, with a focus on quality assurance, validation, and regulatory affairs.