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Lonza in Bend, Oregon, is seeking a site‑based Quality Assurance leader to drive regulatory compliance and reinforce quality systems across GMP production and documentation processes.
You will lead QA teams, collaborate with manufacturing and development, and ensure adherence to internal standards and external inspections. Strong GMP knowledge, leadership, and communication are essential for success in a fast‑paced, regulated environment.
United States, Bend (Oregon)
The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
This role offers an exciting opportunity to lead a high‑performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance, strengthening quality systems, and supporting the delivery of life‑changing therapies.
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.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer 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.