Site Director, Development Quality
Core
Senior leadership role protecting patients and ensuring GMP standards in pharmaceutical development while enabling teams to deliver with pace and confidence.
Role type
Senior IC Site Director, Development Quality
Builds
Development portfolio of investigational products and comparators for clinical trials
Domain
Pharmaceutical Development / GMP / Regulatory Compliance
Required skills
GMP leadership, Quality Assurance, Pharmaceutical Quality Systems, Risk Management, Team Leadership, Regulatory Submissions, Science-based decision making
Preferred skills
Change management, Continuous improvement, Stakeholder influence, Cross-functional collaboration
Technologies
GMP, Quality Systems, Regulatory frameworks
Responsibilities
Set strategic direction for Development Quality function, Lead response to significant compliance issues (recalls, complaints), Sponsor quality improvement initiatives, Ensure high-quality input to development projects and regulatory submissions, Build and lead the local site Quality team, Maintain site pharmaceutical licence
Seniority
Senior, hands-on IC with people leadership
