VP, Global Quality Process Management & Digital Transformation - London, UK
Overview
We are seeking a senior Quality leader to drive the global design, governance, and continuous improvement of end-to-end Quality processes within a large, regulated life sciences environment.
This Vice President role is responsible for establishing and harmonising global Quality process standards across a complex international network, ensuring alignment with regulatory expectations, operational excellence objectives, and digital transformation priorities.
The role partners closely with senior leaders across Quality, Manufacturing, R&D, Regulatory Affairs, Supply Chain, and Digital/Technology functions to simplify and modernise Quality Management System (QMS) processes, strengthen global consistency, and enable inspection-ready operations across all regions.
Key Responsibilities
Own and govern global Quality processes including CAPA, deviations/non-conformances, change control, quality risk management, training, and related QMS processes
Define and maintain global standards, procedures, governance frameworks, and role accountability models to ensure consistent execution
Drive global alignment of Quality processes with regulatory expectations and business priorities across all regions and functions
Lead large-scale simplification, harmonisation, and continuous improvement initiatives to reduce variability, improve efficiency, and strengthen compliance
Oversee digital Quality systems strategy, including eQMS design, workflow optimisation, data standards, and system requirements
Establish global Quality performance frameworks, KPIs, dashboards, and governance routines to support data-driven decision-making
Ensure inspection readiness and support regulatory audits, inspections, and remediation activities through robust process design and governance
Lead cross-functional councils, governance forums, and communities of practice to drive alignment and adoption across a matrixed organisation
Champion change management and capability building to embed standardised global Quality practices
Candidate Profile
Bachelor’s degree in Life Sciences, Engineering, Pharmacy, or a related scientific discipline (advanced degree preferred)
15+ years of experience within pharmaceuticals, biotechnology, medical devices, or another highly regulated industry
Extensive leadership experience in Quality, Quality Systems, Compliance, or related global functions
Proven track record of leading global teams, enterprise processes, or large-scale transformation initiatives
Deep knowledge of GxP regulations and global regulatory frameworks (FDA, EMA, PMDA, MHRA, ICH)
Strong expertise across core QMS areas including CAPA, deviations, change control, investigations, document control, training, and risk management
Experience with digital Quality systems (eQMS), data integrity principles, and inspection-ready environments
Demonstrated ability to influence senior stakeholders and lead in complex, matrixed organisations
Preferred Experience
Leading enterprise Quality transformation or global process ownership initiatives
Implementation or optimisation of large-scale eQMS platforms
Application of Lean, Six Sigma, or operational excellence methodologies
Experience building global governance models, capability frameworks, and communities of practice
Exposure to digital innovation in Quality, including automation, analytics, or AI-enabled capabilities
Travel
Approximately 20–30% international and domestic travel may be required depending on business needs.
Send your updated CV to talent@prestburyinternational.com