Director of Design Quality – Medical Devices Leader

Baxter; Round Lake Beach (IL); Vor Ort; USD 176.000 - 242.000; Vollzeit

Benefits dieser Stelle

Health insurance

401(k) plan

Employee Stock Purchase Plan (ESPP)

Paid time off 20–35 days

Flexible workplace policy

Commuting benefits

Zusammenfassung

Baxter seeks a Director of Design Quality to lead the design quality for infusion systems, pumps, sets, and health software. You will drive quality strategies, partner with regulatory and product teams, and ensure compliance with global standards.

You are a hands-on leader who shapes design quality via KPIs, risk management, and lifecycle activities, delivering safe, high‑quality medical devices in a dynamic environment.

Qualifikationen

• Bachelor's in engineering or related field is required
• 10+ years of experience in quality/engineering/product development
• 7+ years of managerial experience
• Knowledge of medical device regulatory standards and lifecycle

Aufgaben

• Lead a team of Design Quality professionals responsible for product development, lifecycle management, and post-market monitoring
• Develop and implement design quality strategies aligned with goals, standards, and regulatory requirements
• Establish and maintain design quality KPIs and drive continuous improvement
• Provide expertise on design quality to cross-functional teams and external partners
• Collaborate with Quality System stewards to improve the Quality System
• Stay abreast of industry trends and regulatory changes and apply insights
• Represent Baxter in industry forums and standards committees

Kenntnisse

Quality leadership

Regulatory knowledge

Risk management

Quality engineering

Team leadership

Ausbildung

Bachelor's degree in engineering, science, or related field

Advanced degree

Jobbeschreibung

Baxter seeks a Director of Design Quality to lead the design quality for infusion systems, pumps, sets, and health software. You will drive quality strategies, partner with regulatory and product teams, and ensure compliance with global standards.

You are a hands-on leader who shapes design quality via KPIs, risk management, and lifecycle activities, delivering safe, high‑quality medical devices in a dynamic environment.