Project End-to-End; E2E Quality Control Lead

Location & Work Environment

The job is located in Bend, Oregon (USA). This is a fully site‑based role. Relocation assistance is available for eligible candidates and their families, if needed.

• An agile career with opportunities for professional growth and advancement within a global life sciences leader
• A collaborative, inclusive, and purpose‑driven workplace where your contributions make a real difference
• Compensation programs that recognize and reward high performance
• Comprehensive medical, dental, and vision insurance
• Relocation assistance for eligible candidates and their families
• Opportunities to lead impactful, high‑visibility projects that shape the future of QC operations
• Exposure to senior leaders and cross‑functional teams across the organization
• Access to Lonza’s global benefits

• Lead and manage Quality Control project deliverables to ensure compliance with GMP requirements, regulatory expectations, and business objectives
• Oversee the development, qualification, and operational readiness of new QC laboratories, laboratory expansions, and consolidation initiatives
• Serve as the primary QC representative for project teams, Quality Assurance leadership, customers, and regulatory agencies
• Provide quality leadership throughout project life cycles, including deviation management, CAPA implementation, risk assessments, and readiness activities
• Partner with senior leaders to develop and execute project plans, operational readiness strategies, and long‑term QC capabilities
• Monitor project risks, timelines, and compliance challenges; proactively identify solutions and drive successful outcomes
• Champion continuous improvement initiatives by enhancing quality systems, implementing risk management practices, and leveraging performance metrics
• Contribute to the growth and success of a high‑performing QC organization supporting critical patient therapies

• Bachelor’s degree in a scientific discipline required; advanced degree preferred
• Minimum of 5 years of Quality Control experience within a GMP‑regulated pharmaceutical, biotechnology, or life sciences environment
• Strong understanding of QC operations, laboratory compliance, data integrity, and regulatory expectations
• Demonstrated experience leading projects or driving project initiatives in a regulated environment
• Working knowledge of quality systems, including CAPA, audits, investigations, and risk management processes
• Excellent communication, collaboration, and stakeholder management skills
• Proven ability to work cross‑functionally, influence outcomes, and navigate complex organizational environments
• A proactive, solutions‑oriented mindset with a passion for quality and operational excellence

Lonza is a global leader in life sciences operating across five continents. With 30+ sites worldwide, our teams manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion, and Integrity reflect who we are and how we work together. We believe that everyone’s ideas, whether big or small, have the potential to improve millions of lives.

Lonza offers equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.