Process Validation Engineer

About the role

Support medical device manufacturing and injection molding process development.

Tasks

• Develop, optimize, and qualify injection molding processes.
• Independently set up, operate, and troubleshoot large horizontal injection molding presses.
• Apply Scientific Molding and Decoupled III processing techniques.
• Utilize RJG eDART or similar process monitoring systems.
• Execute OQ/PQ activities, analyze results, and prepare qualification reports.
• Coordinate with Operations to manage machine time, project schedules, and deliverables.

Requirements

• Recent hands-on injection molding process development experience within the past 3 years.
• Strong experience in injection molding process optimization and troubleshooting.
• Experience with Decoupled III and RJG eDART or similar systems.
• Medical device industry experience with OQ/PQ process qualifications.
• Experience with Sodick or Sumitomo injection molding presses is preferred.
• Ability to work independently with minimal supervision.
• U.S. Citizens, GC

Schedule

• Duration: 1 Year

How to apply

• Send your updated resume by email.

Location

• Minneapolis, MN