Quality Engineer

Date: Oct 20, 2021

Location: St. Paul – Minnesota, US, 55127

Company: Heraeus

Quality Engineer
Location St. Paul – Minnesota
Full Time

Imagine a job where you will have the opportunity to do exciting and challenging work, while collaborating with extraordinary colleagues. A company that invests in you and your career, providing the training, mentoring, development and support you need to be successful now and in the future. If you want a career without limits with a market-leading family-owned, global company where you can make an impact, then imagine an opportunity at Heraeus. Every day, our worldwide team of around 14,800 employees are bringing forward new ideas and solutions that are impacting and transforming everything from healthcare to renewable energy to e-mobility to high-tech and telecommunications.


Your Role and Responsibilities:

  • Work with process development engineering through all stages of product realization process providing inspection, testing, process characterization support, correlation, DOE, PFMEA, qualifications/validations, GR&R, Minitab analysis, FAI analysis using sound statistical methods.
  • Ensure that proper engineering processes are developed, implemented, maintained and documented to successfully introduce new products that meet the technical needs of our customers
  • Provide direction and quality support for validation of production and test processes. Implement systems and procedures that assure compliance with quality standards/requirements
  • Effectively communicate and document customer needs and associated HMC actions to internal and external stakeholders.
  • Create and review work instructions associated with inspection techniques and inspection equipment and implement improvements that will optimize inspection techniques. Work with internal/external customer to develop inspection methods, process controls and standards for new products.
  • Participates and/or assists with cross training activities, training of new hires and temporary staff. Follows set training program for position and ensures training requirements are up to date.

What is Required for this role

  • BS in Engineering discipline.
  • 3-7  years experience as a Quality Engineer working in a Medical Device manufacturing environment with  ISO 13485:2016 and FDA 21CRF-Part 820.
  • Project management, validation, statistical analysis, Six Sigma Tools and GD&T experience preferred. 

Nearest Major Market: Minneapolis