Director, Quality Programs-Integrated Supply Chain (ISC)

Lead, mentor, and manage a team of Program Managers and data analysts responsible for quality programs. Develop and implement strategic plans for quality programs that align with organizational goals and regulatory requirements. Ensure adherence to industry standards and monitor the effectiveness of quality programs.

10+ years of experience in FDA regulated medical device manufacturing/supply chain environments. Bachelor's degree in Quality, Engineering or a related Scientific discipline required. Strong understanding of Medical Device regulations/standards including ISO 13485/14971, 21CFR, and proven expertise in data analytics.

Company relocation benefits will not be provided for this position. This role requires full-time presence in the company’s facilities, working in-person at least 3 days per week.