Global Quality Transformation Director

Grünenthal Group; Lisboa; Hybrid; EUR 150,000 - 190,000; Full time

Job summary

Grünenthal Group in Lisbon, Portugal seeks a seasoned pharmaceutical Quality leader for our Manufacturing & Global Operations. You will drive quality assessments and lead cross-site diagnostics to uphold the highest standards across the value chain.

The role requires a Master’s in Life Sciences and 15+ years in pharmaceutical quality, with a proven track record in regulatory inspections (FDA/EMA) and major remediation programs.

Qualifications

• 15+ years of experience within pharmaceutical Quality functions.
• Significant experience as Site Head of Quality or Head of QA within GMP environments.
• Proven track record managing remediation programs and quality transformations.

Responsibilities

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

Skills

Quality leadership

GMP experience

Regulatory inspections

Cross-functional leadership

Quality transformation

Mergers & site integrations

Education

Master's degree in Life Sciences or related discipline

Job description

Grünenthal Group in Lisbon, Portugal seeks a seasoned pharmaceutical Quality leader for our Manufacturing & Global Operations. You will drive quality assessments and lead cross-site diagnostics to uphold the highest standards across the value chain.

The role requires a Master’s in Life Sciences and 15+ years in pharmaceutical quality, with a proven track record in regulatory inspections (FDA/EMA) and major remediation programs.