VP Global Quality Assurance - Medical Devices & Surgery

Baxter International Inc.; Deerfield (IL); Vor Ort; USD 280.000 - 410.000; Vollzeit

Benefits dieser Stelle

Medical and dental coverage

401(k) with company matching

Paid holidays and PTO 20–35 days

Zusammenfassung

Baxter International Inc. is seeking a Vice President, Global Quality Assurance for MDS to set strategic direction and lead global quality across multiple medical device businesses.

You will build governance, ensure regulatory compliance, and drive quality improvements across development, manufacturing, and post-market activities. Key responsibilities include partnering with regulators and cross-functional teams, guiding risk-based decisions, and developing a diverse, capable global Quality

Qualifikationen

• 15+ years in Quality, Engineering, Manufacturing, or related field in regulated industry.
• 10+ years in progressively senior Quality or Operations leadership roles.
• Executive-level experience leading global, matrixed Quality organizations.
• Deep medical device knowledge across product development to post-market.
• Strong knowledge of FDA QSR, EU MDR, ISO 13485 and ISO 14971.

Aufgaben

• Set global MDS Quality strategy, governance, and operating model.
• Lead quality across three medical device businesses and portfolios.
• Advance scalable Quality Management Systems for compliance and innovation.
• Direct risk decisions and escalation for quality, safety, or supply risks.
• Collaborate with regulators and cross-functional teams for inspections and remediation.

Kenntnisse

Quality leadership

Regulatory compliance

Global matrix leadership

Decision making

Regulatory liaison

Ausbildung

Master's degree

Tools

QMS (ISO 13485/ISO 14971)

Jobbeschreibung

Baxter International Inc. is seeking a Vice President, Global Quality Assurance for MDS to set strategic direction and lead global quality across multiple medical device businesses.

You will build governance, ensure regulatory compliance, and drive quality improvements across development, manufacturing, and post-market activities. Key responsibilities include partnering with regulators and cross-functional teams, guiding risk-based decisions, and developing a diverse, capable global Quality