Wendy Summers
About Wendy Summers
Title: Vice President of Pharmaceutical Operations and Technology
Wendy Summers currently holds the title of Vice President of Pharmaceutical Operations and Technology. In this role, she oversees key operational aspects and technological initiatives within the pharmaceutical domain, ensuring that processes adhere to industry standards and improve efficiency and efficacy in drug development.
Education: B.S. in Pharmaceutical Sciences from Campbell University
Wendy Summers earned a Bachelor of Science in Pharmaceutical Sciences from Campbell University. This educational foundation has provided her with a comprehensive understanding of pharmaceutical sciences, equipping her with the knowledge necessary to excel in various roles within the pharmaceutical industry.
Previous Positions: Head of Research and Development QA for Novartis Gene Therapies
Wendy Summers was the Head of Research and Development Quality Assurance (QA) for Novartis Gene Therapies. In this role, she was responsible for ensuring that the research and development processes met rigorous quality standards. Her work supported the compliance and regulatory requirements essential for gene therapy products.
Past Experience: Head of Quality for Chiesi, USA
Wendy held the position of Head of Quality for Chiesi, USA. During her tenure, she was tasked with overseeing quality assurance and control processes. Her responsibilities included the management and enhancement of quality systems to ensure that the products met both regulatory and internal standards.
Regional QA Roles: UCB and Biogen
Wendy Summers has extensive experience in regional Quality Assurance (QA) roles at UCB and Biogen. Her roles included managing QA operations and ensuring compliance with regulatory standards across multiple regions. Her work affected QA processes in the United States, Europe, and Asia.
Team Building: Experience in the US, EU, and Asia
Throughout her career, Wendy Summers has built and led teams across the United States, European Union, and Asia. Her leadership capabilities have been demonstrated in her ability to form teams that effectively support the organizational goals and regulatory requirements in diverse geographical regions.
Regulatory Support for Biologic and Gene Therapy Products
Wendy Summers has supported numerous regulatory licenses for biologic and gene therapy products. Her involvement in these processes ensures that the products comply with regulatory standards, facilitating their approval and market entry. Her contributions have been critical in navigating the complex regulatory landscape for these advanced therapies.