Quality Transformation & Site Excellence Lead

Grünenthal Group; Santiago; Teletrabalho; CLP 146 771 000 - 244 618 000; Tempo integral

Resumo da oferta

Grünenthal Group is seeking an accomplished Quality leader to drive assessments, diagnostics, and strategic transformations across global manufacturing sites. You will guide remediation efforts, oversee regulatory interactions, and shape comprehensive quality programs to sustain compliance and excellence.

The role requires extensive experience in pharmaceutical quality, a track record with FDA/EMA inspections, and the ability to lead multi-site initiatives while driving cultural change and

Qualificações

• 15+ years of experience in pharmaceutical Quality functions.
• Proven experience supporting FDA, EMA and international regulatory inspections.
• Track record managing complex remediation programs and quality transformations.
• Experience leading cross-functional and multi-site initiatives within global pharma organizations.
• Experience in mergers, acquisitions, site integrations or large-scale organizational change is advantageous.

Responsabilidades

• Lead quality assessments and diagnostics at manufacturing sites.
• Provide hands-on support to sites facing compliance, inspection, performance, or quality system challenges.
• Serve as interim Quality leader or advisor during critical business situations, leadership transitions, or remediation programs.
• Lead regional quality transformation programs and strategic improvement projects.
• Ensure sustainable resolution of quality risks, deviations, audit findings, and systemic compliance gaps.
• Coach and develop site Quality leaders and quality teams.
• Strengthen quality culture and continuous improvement capabilities at site leadership level.

Conhecimentos

Quality leadership

Regulatory inspections

Remediation programs

Cross-functional leadership

Change management

Descrição da oferta de emprego

Grünenthal Group is seeking an accomplished Quality leader to drive assessments, diagnostics, and strategic transformations across global manufacturing sites. You will guide remediation efforts, oversee regulatory interactions, and shape comprehensive quality programs to sustain compliance and excellence.

The role requires extensive experience in pharmaceutical quality, a track record with FDA/EMA inspections, and the ability to lead multi-site initiatives while driving cultural change and