Senior Director of Quality

Responsibilities

• Provide strategic leadership for the Quality Management System, ensuring compliance with FDA regulations, ISO 13485, and international quality standards.
• Lead and mentor teams across Quality Systems, Quality Engineering, Supplier Quality, Design Assurance, and Post-Market Surveillance.
• Partner closely with R&D, Regulatory Affairs, Clinical Affairs, Manufacturing, and Operations.
• Serve as the primary Quality representative during FDA inspections, notified body audits, and MDSAP audits.

Qualifications

• Deep understanding of FDA Quality System Regulations, ISO 13485, ISO 14971, and global medical device compliance requirements.
• Prior experience within cardiovascular, structural heart, electrophysiology, neurovascular, or other Class III implantable medical device environments.
• Strong expertise in design controls, risk management, CAPA, supplier quality, process validation, complaint handling, and post-market quality systems.
• Demonstrated success leading Quality organizations through product development, clinical studies, commercialization, and regulatory inspections.

Benefits

• Competitive executive compensation package
• Long-term incentive plan (LTIP), equity, and stock options
• Comprehensive medical, dental, and vision coverage
• 401(k) with company match
• Opportunity to make a significant impact within a high-growth, innovative medical device organization