Senior Director Quality

We believe that great healthcare is an essential safeguard of human dignity.

At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.

We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

As a key member of the Quality team, the Senior Director Quality will be responsible for developing, implementing, and continuously improving the organization's Product Quality and Production Quality programs across the medical device lifecycle. This position ensures compliance with global regulatory requirements, quality management system (QMS) standards, and company objectives while driving a culture of quality, operational excellence, and patient safety.

The role provides leadership for product quality assurance, manufacturing quality, supplier quality, risk management, and continuous improvement initiatives.

• Develop and execute the quality strategy aligned with corporate goals and regulatory requirements.
• Lead and mentor Product and Manufacturing Quality teams across multiple sites and/or regions.
• Establish quality objectives, key performance indicators (KPIs), and continuous improvement plans.
• Drive a culture of quality, compliance, customer focus, and operational excellence throughout the organization.

• Oversee product quality throughout design transfer, manufacturing, commercialization, and post-market activities.
• Ensure robust quality oversight of design changes, process changes, and product lifecycle management activities.
• Lead investigations and resolution of product quality issues, nonconformances, customer complaints, and field actions.
• Ensure effective implementation of risk management processes consistent with ISO 14971 requirements.
• Monitor and analyze quality data, complaint trends, field performance, and reliability metrics to drive product improvements.
• Partner with R&D and Regulatory Affairs to support product development and design validation activities.

• Provide leadership for manufacturing quality systems, including incoming inspection, in-process controls, final release, and quality engineering.
• Ensure effective control of manufacturing processes, validation activities, and process monitoring systems.
• Lead quality oversight of production operations to ensure compliance with FDA Quality System Regulation (QSR), ISO 13485, and other applicable standards.
• Drive reduction of scrap, rework, defects, and manufacturing nonconformances through data-driven quality initiatives.
• Support operational excellence and Lean/Six Sigma programs to improve efficiency and product quality.

• Act as a primary quality representative during FDA inspections, notified body audits, and customer audits in conjunction with other Quality leadership.
• Ensure timely responses to audit observations and regulatory findings, particularly as they relate to products and manufacturing.
• Support regulatory submissions and product approvals as required.

• Utilize quality metrics, statistical techniques, and quality engineering tools to improve product and process performance.
• Lead root cause investigations and implementation of effective corrective and preventive actions.
• Promote use of Lean, Six Sigma, and risk-based approaches throughout quality and manufacturing operations.
• Identify opportunities for automation, process simplification, and digital quality transformation.

• Lead, coach, and develop quality management professionals and technical teams.
• Build organizational capabilities through talent development and succession planning.
• Foster…