The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
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 do- You will support capital projects from design through commissioning and startup
- You will participate in planning, risk assessments, and design reviews
- You will improve equipment reliability and long-term performance
- You will analyze downtime and maintenance data to drive improvements
- You will support maintenance strategies, including preventive and predictive programs
- You will collaborate with cross-functional teams and external partners
- You will ensure compliance with cGMP and industry standards
What we are looking for- You bring a degree in engineering or a related technical field, or equivalent experience
- You have strong experience in biotechnology, pharma, or manufacturing environments
- You have experience supporting capital projects and equipment lifecycle performance
- You understand reliability tools such as FMEA, root cause analysis, or similar methods
- You can manage multiple priorities in a fast-paced, cross-functional environment
- You communicate effectively and build strong working relationships
- You are detail-oriented and committed to quality, safety, and compliance
