David V.
About David V.
David V. serves as the Vice President of Quality at EyePoint Pharmaceuticals, bringing over two decades of experience in quality assurance and regulatory compliance within the pharmaceutical and medical device industries.
Work at EyePoint Pharmaceuticals
David V. serves as the Vice President of Quality at EyePoint Pharmaceuticals since 2021. In this role, he oversees quality assurance and compliance operations, ensuring that the company's products meet regulatory standards. His leadership contributes to the development and implementation of quality management systems that align with industry regulations.
Previous Experience in Quality and Regulatory Roles
Prior to his current position, David V. held several significant roles in quality and regulatory affairs. He worked at Tedor Pharma, Inc. as Vice President of Quality & Regulatory for one year, and at Foster Delivery Science in similar roles for two years. His experience includes positions at Pfizer, Lantheus Medical Imaging, ImmunoGen, Inc., Bristol-Myers Squibb, and Abbott, where he focused on quality assurance and compliance.
Education and Expertise
David V. earned a Bachelor of Science degree from Northeastern University, studying Mechanical Engineering Technology from 1982 to 1987. He also obtained a Certificate in PC Network Administration from Daniel Webster College between 1996 and 1998. His educational background supports his extensive expertise in quality management, regulatory compliance, and process improvement methodologies, including lean and six sigma.
Achievements in Quality Management
David V. has extensive experience in architecting and implementing global harmonized automated Quality Management Systems. He is recognized for his ability to develop effective systems that enhance quality assurance processes. His technical and business background includes defining user and functional requirements, managing system implementations, and developing internal procedures to meet compliance standards.
Regulatory Knowledge and Compliance
David V. possesses a solid technical background in compliance and regulatory affairs, particularly within the pharmaceutical, biologics, and medical device sectors. He is knowledgeable about FDA regulations, including 21CFR820, 210, 211, 600, and 11. His expertise in these areas positions him as a champion for quality within the organizations he has served.