Daniel Butterfield
About Daniel Butterfield
Daniel Butterfield serves as the Associate Director of Quality Assurance at Avyxa Pharma, where he has worked since 2024. He has extensive experience in quality assurance and regulatory compliance within the pharmaceutical industry, having held various positions at multiple companies over the years.
Current Role at Avyxa Pharma
Daniel Butterfield serves as the Associate Director of Quality Assurance at Avyxa Pharma, a position he has held since 2024. He works in Parsippany, New Jersey, where he is responsible for overseeing quality assurance processes and ensuring compliance with industry standards. His role includes acting as a designated representative for audits and inspections by regulatory agencies, which is critical for maintaining the company's operational integrity.
Previous Experience in Quality Assurance
Before his current role, Daniel Butterfield worked at Ingenus Pharmaceuticals as a Senior Quality Assurance Manager from 2021 to 2024. In this capacity, he managed quality assurance protocols and compliance measures in Orlando, Florida. He also held positions at RiconPharma LLC, where he served as Quality Assurance Manager and later as Senior Manager - QA from 2018 to 2024, contributing to quality management initiatives in Denville, New Jersey.
Educational Background in Biochemistry
Daniel Butterfield earned a Bachelor of Science (B.S.) degree in Biochemistry and Molecular Biology from Penn State University. His studies spanned from 2005 to 2011, providing him with a strong foundation in the scientific principles that underpin his work in the pharmaceutical industry.
Experience in Pharmaceutical Industry
Daniel has extensive experience in the pharmaceutical sector, having worked in various roles that include R&D Chemist at Teva Pharmaceuticals and Quality Control Chemist at ULTRA TAB LABORATORIES INC. His career also includes a supervisory role at Akorn, Inc., where he managed raw materials. His diverse background equips him with a comprehensive understanding of quality assurance and regulatory compliance.
Special Projects and Regulatory Compliance
In his various roles, Daniel Butterfield has coordinated specialty projects with executive teams to ensure the efficient establishment of business activities. He oversees site quality procedures related to current Good Manufacturing Practices (cGMP), vendor management, pharmacovigilance, and distribution, ensuring that all operations align with federal and state regulations. His responsibilities also include establishing registrations and licenses necessary for launching products in a start-up specialty pharmaceutical environment.