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Process Engineer

Job in Eugene, Lane County, Oregon, 97403, USA
Listing for: Kaye/Bassman International
Full Time position
Listed on 2026-08-22
Job specializations:
  • Engineering
    Process Engineer, Validation Engineer, Manufacturing Engineer, Quality Engineering
  • Manufacturing / Production
    Validation Engineer, Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Our client is a U.S.

-based contract development and manufacturing organization (CDMO) specializing in small-molecule active pharmaceutical ingredient (API) development and manufacturing. The organization recently expanded its footprint through the acquisition of a longstanding cGMP manufacturing site in the Pacific Northwest, adding a 30,000-square-foot manufacturing facility to its network.

The site has operated as a drug substance manufacturer for over 40 years and has built a reputation for deep technical expertise in early-phase API development and scale-up.

“A CDMO worth watching — quietly building one of the most technically capable API platforms on the West Coast.” — Industry Trade Press

2.

The Role They Will Play

The Process Engineer will be the technical backbone of a cGMP manufacturing site, translating process science into reliable, compliant production — the difference between a batch that ships and one that doesn't.

Day to day, this means troubleshooting reactors, chillers, filter dryers, and TCUs; scaling up new processes from development into operations; and driving continuous improvement across the site's equipment and procedures.

Unlike a pure R&D role, this position sits at the intersection of development and operations — equal parts scientist, engineer, and problem-solver, with direct exposure to client-facing CDMO work.

For the right candidate, this is a launchpad into site engineering leadership as the facility continues to grow under new ownership.

We're looking for a hands-on process engineer who thrives in a regulated manufacturing environment and is ready to be the go-to technical resource on the floor.

  • Expertise in cGMP pharmaceutical or API manufacturing processes.
  • 5+ years' experience in process/manufacturing engineering (or 10+ years' relevant experience with a non-engineering degree).
  • Exposure to batch chemical reactors, filter dryers, TCUs, pumps, and related process equipment.
  • Working knowledge of process control and data collection systems (PLC, SCADA).
  • BS in Chemical, Mechanical, or related Engineering, or equivalent experience.
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