Senior Process Development Engineer
Canton, IL (onsite )
Contract :- 12 MONTH
Please note: **All candidates must be U.S. Citizens or Green Card holders.**
I'm reaching out because I need your support on a new Process Development opportunity with our client, located in Canton, IL. This is a year-long contract role, with the possibility of extension or even conversion to direct hire.
Please note: **All candidates must be U.S. Citizens or Green Card holders.**
Below are the key details for the position:
Job Responsibilities:
• Lead development, validation, and implementation of manufacturing processes for new medical devices
• Collaborate closely with R&D, Operations, Quality, and Regulatory teams
• Apply principles of Design for Manufacturability, Lean, and risk-based process development
• Drive Make vs. Buy analysis and support supplier selection
• Own key process documentation (PFMEAs, instructions, drawings, etc.)
• Contribute to successful transfer of devices from development to sustaining production
Desired Qualifications:
• Bachelor's degree in Engineering
• 5+ years' experience in Class II/III medical device manufacturing
• Strong background in process validation, ISO 13485/FDA requirements, GMP, and Lean
• Experience collaborating in multidisciplinary teams
• Excellent communication and project leadership skills
There will be two interview rounds for this role. If you have strong candidates who would be a good fit, please send them my way. I appreciate your partnership and look forward to working together on this important search.