Director, Process Excellence & Quality Compliance

Philips International

Cambridge (MN)

Hybrid

USD 180.000 - 260.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Philips seeks a Director, Process Compliance & Centers of Excellence to lead enterprise quality controls, drive process improvements, and oversee documentation and regulatory compliance across global sites.

You will guide PFMEA, design transfer, NPI validations, CAPA, NC, and QN processes, mentor quality engineers, and partner with R&D, manufacturing and regulatory affairs to reduce COPQ and achieve superior quality standards.

Qualifikationen

  • Drive strategic initiatives to elevate supplier quality standards, collaborating with R&D, manufacturing and regulatory affairs to address process gaps.
  • Guide setup of acceptance activities, transfer to manufacturing, NPIs validations, process development and control plans.
  • Collaborate with Quality Optimization to integrate initiatives into site QMS processes.
  • Lead cost reduction and productivity through COPQ data analysis and support cost-saving initiatives.
  • Lead regulatory inspections (FDA, Notified Bodies) and ensure compliance with global standards.
  • Bachelor’s degree in Engineering/Life Sciences required; Master’s preferred.

Aufgaben

  • Drive strategic initiatives to elevate supplier quality standards and collaborate with cross-functional teams to address process gaps.
  • Analyze data to identify trends, risks, and improvement opportunities and support process improvements.
  • Oversee PFMEA assessments and relate controls to design changes; support NPI projects and product transfers.
  • Mentor and develop a high-performing team aligned with organizational goals.

Jobbeschreibung

Philips seeks a Director, Process Compliance & Centers of Excellence to lead enterprise quality controls, drive process improvements, and oversee documentation and regulatory compliance across global sites.

You will guide PFMEA, design transfer, NPI validations, CAPA, NC, and QN processes, mentor quality engineers, and partner with R&D, manufacturing and regulatory affairs to reduce COPQ and achieve superior quality standards.

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