Vice President of Quality

The Company is seeking a Vice President of Quality to set the organization’s quality vision and strategy and guide its next phase of growth. The role oversees quality across product development, manufacturing, supplier management, post-market activities, and global operations, ensuring compliance while fostering a culture of quality and patient safety. Responsibilities include leading quality systems, design and supplier quality, manufacturing quality, complaint handling, and post-market surveillance. The VP will partner with executive leadership and cross-functional teams to support innovation, commercialization, and global expansion. Candidates should hold a bachelor’s degree in engineering, life sciences, biomedical engineering, or a related technical field, with at least 15 years of quality experience in the medical device industry and seven years leading quality organizations and cross-functional teams. Demonstrated success in Class III and other highly regulated device environments is required. Applicants should bring expertise in FDA quality regulations, ISO 13485, MDR, MDSAP, CAPA, risk management, supplier quality, and design controls. Experience supporting products from development through approval, commercialization, and post-market activities, leading inspections and audits, and scaling quality organizations is also required.