About this role
About the Role Director of Global Innovation Quality Compliance Clinical is responsible for developing and refining global manufacturing quality processes, leading implementations, and training site teams with cross-functional collaboration under Global Practice Area leads. The role drives global process improvements and continuous improvement initiatives across manufacturing sites. What You'll Do
- Identify and define global processes (30%): collect expectations and requirements for core manufacturing quality processes, determine gaps, and develop a global quality manufacturing framework, processes, procedures and tools aligned with stakeholder requirements, with cross-functional collaboration.
- Drive implementation of global process improvements (50%): evaluate risks, define action plans, project manage site-level implementations, and provide training to local Quality and Operations with site and COE training teams.
- Establish and manage continuous improvement processes (20%): incorporate best practices globally, drive continuous improvement of quality processes, implement lean/CI practices focusing on Quality and process control, and conduct routine reviews with VP/Regional Quality Leads to adapt as needed. What We're Looking For
- Experience in a fast-paced consumer goods manufacturing environment (cosmetic, food, or pharma) is a plus.
- Strong knowledge of Continuous Improvement and Lean methodology.
- Ability to conduct and train on risk assessment and root cause analysis.
- Data analytics, statistics and process control proficiency.
- Excellent project management, communication, and stakeholder management.
- Strong technical writing skills; ability to write and review SOPs and communicate across cross-functional teams.
- Proficiency with Microsoft Office and SAP.
- Knowledge of ISO certification highly preferred. Nice to Have
- ISO certification knowledge preferred. Compensation & Benefits
- Salary: Not disclosed (USD).