Quality Engineer

Company:  HOYA Vision Care
Location: Ramsey
Closing Date: 03/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Join The Hoya Vision Care Team!
For over 60 years, HOYA Vision Care has been a passionate leader in optical technology innovation. As a manufacturer of high quality, high performing eyeglass lenses, we continuously aim to bring the best possible vision care solutions to eye care professionals.
We are currently hiring a Quality Engineer in Ramsey, MN
What's in it for you?
  • Health/Dental/Vision/Disability Insurance
  • Tuition Reimbursement
  • 401K plans
  • PTO and Paid Holidays
  • And more!
What you'll do:
  • Work closely with the project management team to ensure that our medical devices meet regulatory and quality requirements
  • Collaborate with cross functional teams and other departments to provide quality leadership, guidance and support in design control methodologies for medical device designs
  • Conduct risk assessments and participate in design failure mode and effects analysis (DFMEA) activities
  • Develop documentation (i.e. quality plans, procedures) to ensure compliance with applicable regulations
  • Participate in the development of product validation plans and support product validation testing
  • Support the Quality and Metrology Manager with QMS maintenance and development
  • Perform internal QMS audits to ensure compliance with quality requirements
  • Support the Quality Manager with external audits (i.e. ISO 9001, ISO 13485, FDA)
  • Investigate and document non-compliances, identify root causes, and develop corrective and preventive actions
Qualifications:
  • Bachelor's degree in engineering, Science, or related field
  • 2+ years hands-on experience in medical device quality engineering
  • Experience with FDA regulated products and ISO 13485 certified QMS
  • Experience in product development including implementing appropriate controls
  • Working knowledge of statistics is required, with Six Sigma Green Belt (or higher) certification being a plus
  • Working knowledge of FDA regulations (21 CFR 820) and other relevant standards is strongly preferred
  • Experience in performing QMS audits is preferred, with ASQ certification as a Quality Auditor being a plus
  • Experience in a medical device start-up environment is a plus
  • Experience with risk management tools, design controls, and process validation (IQ/OQ/PQ) is a plus
  • Experience in optics/ophthalmic is a plus
  • Proficiency with Minitab, MS Outlook, MS Word, and MS Excel
Other details
  • Pay Type Salary

Apply Now
Apply Now
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