Partner with engineering, QA, and manufacturing teams to support smooth project execution.
Troubleshoot and improve equipment, processes, and systems.
Write, review, and execute qualification protocols (IQ/OQ/PQ) for new and existing equipment.
Identify risks to product quality and apply mitigation strategies.
Generate validation reports and maintain compliant documentation following FDA and cGMP guidelines.
Manage and close deviations or non‑conformances identified during testing.
Support engineering documentation such as user requirements and design qualification materials.
Requirements
High School Diploma or GED required; engineering degree preferred.
Experience in CQV and temperature mapping.
Understanding of FDA, ICH, ISPE, and ISO guidelines.
Proficiency with Microsoft Word and Excel.
Ability to solve problems and work cross‑functionally.
Strong communication and documentation skills.
Interest in improving systems and supporting safe, effective drug development.
Ready to shape the future of life sciences?
Benefits
Dental insuranceVision insurance
Additional Information
The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
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.
Lonza · Us - Bend, OR