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Process Engineer

Job in Eugene, Lane County, Oregon, 97401, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-09-01
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer, Quality Engineering, Validation Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Validation Engineer
Job Description & How to Apply Below

Process Engineer

CBS LLC is seeking an experienced Process Engineer to provide manufacturing and sustaining engineering support within a regulated manufacturing environment, with a focus on process optimization, validation, equipment qualification, and continuous improvement.

Roles & Responsibilities:

  • Provide manufacturing and sustaining engineering support for production operations.
  • Drive process improvements, yield enhancement, equipment optimization, and manufacturing solutions.
  • Develop and optimize manufacturing processes to meet quality, cost, productivity, and compliance objectives.
  • Collaborate with R&D, Product Development, Quality, and Operations teams on NPI and Design Transfer activities.
  • Perform process validation, statistical analysis, and equipment qualification.
  • Support equipment selection, installation, commissioning, and qualification activities.
  • Ensure manufacturing processes comply with applicable regulatory and quality requirements.
  • Lead moderately complex engineering projects and support achievement of project milestones.
  • Drive continuous improvement initiatives and manufacturing efficiency.
  • Provide technical guidance and mentorship to junior engineers when required.

Required Skills:

  • Process Engineering
  • Manufacturing & Sustaining Engineering
  • SPC – Statistical Process Control
  • Process Validation
  • Equipment Qualification
  • Manufacturing Process Development
  • Yield Improvement
  • Equipment Optimization
  • Statistical Analysis
  • NPI / New Product Introduction
  • Design Transfer
  • Continuous Improvement
  • Regulated Manufacturing
  • Medical Device / Pharmaceutical Manufacturing
  • Quality & Regulatory Compliance
  • Engineering background with hands-on experience in regulated manufacturing
  • Strong analytical, problem-solving, and project management skills
  • Experience working cross-functionally with R&D, Quality, Operations, and Product Development teams
  • Ability to independently manage moderately complex engineering projects
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