The actual location of this job is in Bend, Oregon, United States. Relocation assistance is available for eligible candidates and their families, if needed
In this role, you will lead a high-performing analytical chemistry team, ensuring quality, compliance, and continuous improvement in a dynamic GMP environment.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance.
- Medical, dental, and vision insurance.
- Access to Lonza's global benefits program.
- Opportunities to lead and develop high-performing teams.
- Exposure to strategic site initiatives and growth projects.
What you will do:- Build and manage daily laboratory schedules to meet operational needs.
- Review and approve analytical test documentation and reports.
- Represent the team during client audits and regulatory inspections.
- Assign projects and continuous improvement tasks, tracking progress.
- Lead team performance, development, and training compliance.
- Identify and implement process improvements to enhance performance.
- Support capital investment (CAPEX) and site growth initiatives.
What we are looking for:- Bachelor's degree in a scientific field.
- Experience leading teams in a pharmaceutical QC environment.
- Strong knowledge of Good Manufacturing Practices (GMP) and documentation standards.
- Ability to lead with integrity, respect, and professionalism.
- Comfortable working in a fast-paced, detail-oriented environment.
- Strong communication and organizational skills.
