Global Quality Process Leader | CAPA, Change & Digital

Biopharma Careers

Antwerpen

Hybrid

EUR 120.000 - 180.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Johnson & Johnson seeks a Head of Global Process Management to lead end-to-end quality processes, including CAPA, deviations, and change control, across a global network. You will translate strategy into clear standards and performance metrics, partnering with Quality, Manufacturing, R&D, Regulatory, and Supply Chain to drive improvements.

The role requires extensive experience in regulated environments, strong stakeholder influence, and the ability to manage digital workflows and eQMS

Qualifikationen

  • Bachelor’s degree in life sciences, engineering, pharmacy, or related scientific discipline.
  • At least 12 years of progressive experience in pharmaceuticals, biotechnology, medical devices, or another highly regulated industry.
  • At least 7 years of people management experience, including leadership of global teams.

Aufgaben

  • Lead design, governance, digital enablement, and continuous improvement of global Quality processes (CAPA, deviations, non-compliance).
  • Translate enterprise quality strategy into standards, governance, and performance measures.
  • Partner with Quality, Manufacturing, R&D, Regulatory, Supply Chain, and Digital/IT to drive adoption and outcomes.

Kenntnisse

Quality Systems
CAPA
Change Control
GxP Knowledge
Regulatory Knowledge
Data Integrity
Stakeholder Management
Executive Communication
Lean Six Sigma
Digital Quality

Ausbildung

Bachelor's Degree in Life Sciences/Engineering/Pharmacy
Advanced Degree (MBA/PhD/PharmD)

Tools

eQMS Platforms

Jobbeschreibung

Johnson & Johnson seeks a Head of Global Process Management to lead end-to-end quality processes, including CAPA, deviations, and change control, across a global network. You will translate strategy into clear standards and performance metrics, partnering with Quality, Manufacturing, R&D, Regulatory, and Supply Chain to drive improvements.

The role requires extensive experience in regulated environments, strong stakeholder influence, and the ability to manage digital workflows and eQMS

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