Senior Manufacturing Engineer

Plymouth, MN, US • Posted 2 hours ago • Updated 2 hours ago
Contract Independent
Contract W2
12 Months
On-site
$50 - $60/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • ISO 13485
  • GMP
  • Medical Devices
  • Regulatory Compliance
  • Root Cause Analysis
  • Corrective And Preventive Action
  • DMAIC
  • Process Engineering
  • Manufacturing

Summary

Role:Sr. Manufacturing Engineer
Location:Plymouth, MN

Key Responsibilities:
Lead yield improvement and continuous improvement initiatives across manufacturing processes
Troubleshoot and resolve process issues using DMAIC, RCA, and data-driven methodologies
Support catheter manufacturing processes including assembly, bonding, soldering, reflow, stringing, and packaging
Support NPI, process scale-up, and technology transfer activities
Collaborate with Quality, R&D, Operations, and Regulatory teams
Ensure compliance with FDA, ISO 13485, and GMP requirements
Mentor junior engineers and support cross-functional project execution

Required Qualifications:
5+ years of manufacturing/process engineering experience
Strong medical device manufacturing background
Experience with catheter manufacturing processes preferred
Knowledge of FDA, ISO 13485, GMP, CAPA, and process validation

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10238807
  • Position Id: 8972636
  • Posted 2 hours ago
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