Process Engineer Ii

Integer

Plymouth, MN, United States
Base: $79,000 - $116,160; bonus/equity: cash-based...
**
Quality management systems (qms)
Root cause analysis and data analysis
New product and process development
** Integer is seeking a Process Engineer II to contribute to new product/process development within the medical device industry. The role emphasizes collaboration, quality management, and continuous improvement, with a focus on meeting customer expectations and adhering to regulatory standards. **

Job Summary

  • Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEMs and specialized battery markets, guided by six core values including Customer focus, Innovation, and Integrity.
  • The role involves leading new product and process development projects, applying engineering techniques to ensure quality and regulatory compliance, and driving manufacturing excellence through continuous improvement initiatives.
  • Employees receive a comprehensive benefits package with immediate eligibility, including medical, dental, vision, life insurance, 401(k) with company match, paid time off, and parental leave after one year.

Matching Summary

Match Score: 75

** Integer is seeking a Process Engineer II to contribute to new product/process development within the medical device industry. The role emphasizes collaboration, quality management, and continuous improvement, with a focus on meeting customer expectations and adhering to regulatory standards. **

Salary

Base: $79,000 - $116,160; Bonus/Equity: Cash-based incentive program; Benefits: Medical, dental, vision, disability, life insurance, 401(k) with company match, paid time off

Skills & Requirements

Must-have

  • Quality Management Systems (QMS)
  • Root cause analysis and data analysis
  • New product and process development
  • Manufacturing Excellence and continuous improvement
  • Adherence to FDA regulations
  • Collaboration with cross functional teams

Nice-to-have

  • Positive, can-do attitude
  • Calm demeanor in high energy environment
  • Effective written and oral communication
  • Proactive insight into technical challenges
  • Champion innovation and continuous improvement
  • Standard bearer for quality

Key Requirements

  • Bachelor’s degree in engineering or related technical field
  • Minimum three years relevant experience or seven years without degree
  • Functional understanding of Quality Management Systems
  • Ability to work independently and collaboratively
  • Compliance with FDA and regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter