1

Temp Quality Engineer Medical Device Jobs in Minnesota

Ability to grow your career within a rapidly evolving medical device organization. * Mission-driven ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

next page

Showing results 1-20

Temp Quality Engineer Medical Device information

What is the difference between Temp Quality Engineer Medical Device vs Temp Quality Technician Medical Device?

AspectTemp Quality Engineer Medical DeviceTemp Quality Technician Medical Device
CredentialsBachelor's in Engineering, Quality or related field; certifications like CQE often preferredHigh school diploma or associate degree; technical certifications beneficial
Work EnvironmentDesign, develop, and improve quality systems; collaborate with engineering teamsPerform inspections, testing, and documentation; support quality assurance processes
Employer & Industry UsageUsed in medical device manufacturing companies for process developmentCommonly employed in quality control labs and manufacturing lines

The Temp Quality Engineer Medical Device focuses on developing and improving quality systems, requiring more technical expertise and engineering knowledge. In contrast, the Temp Quality Technician Medical Device primarily handles testing, inspections, and documentation tasks. Both roles are essential in ensuring product quality but differ in responsibilities and required qualifications.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Minnesota?

The most popular types of Quality Engineer Medical Device jobs in Minnesota are:

What cities in Minnesota are hiring for Temp Quality Engineer Medical Device jobs?

Cities in Minnesota with the most Temp Quality Engineer Medical Device job openings:

Quality Engineer Medical Device

Roseville, MN • On-site

Egg Medical Inc
Manufacturing • 1 - 10 employees

$100K - $115K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago


Job description

Summary

We are seeking a Quality Engineer to add to our team! This position will support the management of our quality system while actively contributing to new product design and development initiatives. This role combines core quality engineering responsibilities with technical involvement in engineering projects to ensure our innovative medical devices meet the highest standards of safety, reliability, and regulatory compliance. 

Key Responsibilities

  • Quality System Support: Develop, implement, and maintain elements of the Quality Management System (QMS) to ensure ongoing compliance with FDA regulations, ISO 13485, and other applicable standards.
  • New Product Development & Design Control: Collaborate with R&D, engineering, and cross-functional teams on new design projects; support design inputs/outputs, risk assessments (e.g., FMEA, ISO 14971), design verification and validation activities, and design reviews/transfer to manufacturing.
  • Risk Management & Technical Reviews: Perform and document risk analyses, participate in technical design reviews, and ensure design controls are effectively applied throughout the product lifecycle.
  • Non-Conformance & Corrective Actions: Investigate non-conformances, lead root cause analysis, and implement corrective and preventive actions (CAPA) to drive continuous improvement and prevent recurrence.
  • Documentation & Compliance: Maintain accurate quality records, support internal/external audits, and contribute to regulatory submissions as needed.
  • Continuous Improvement: Identify opportunities to improve quality processes, product designs, and overall efficiency; partner with engineering and other teams on quality initiatives

Qualifications

  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Quality Engineering, or a related field.
  • 3+ years of experience as a Quality Engineer in a regulated industry, preferably medical devices.
  • Experience with FDA regulations, ISO 13485, and other medical device quality standards.
  • Proficiency in quality tools and methodologies (e.g., FMEA, SPC, CAPA).

Compensation & Benefits

  • Full-time position with salary range from $100,000-$115,000, depending on experience.
  • Additional bonus/incentive compensation available.
  • Company laptop provided.
  • Insurance available on the 1st of the month following date of hire, including: health, dental and vision insurance, plus pre-tax or Roth 401k available after 30 days.
  • PTO accrues starting at 15 days, plus 11 company paid holidays.

Company Description

Egg Medical is an innovative leader in radiation safety protection technology. Our mission is to protect healthcare professionals from occupational radiation exposure while enabling the delivery of exceptional patient care.