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Quality Engineer

Job in Big Lake, Sherburne County, Minnesota, 55309, USA
Listing for: TOMZ Corporation
Full Time position
Listed on 2026-10-30
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 85000 - 102000 USD Yearly USD 85000.00 102000.00 YEAR
Job Description & How to Apply Below

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Quality Engineer

QUALITY Full Time Big Lake, MN, US

2 days ago Requisition

Salary Range: $85,000.00 To $ Annually

TOMZ in Big Lake is looking for a Quality Engineer to join our team!! Reporting to the Quality Engineering Manager, this position will be responsible for the activities associated with Quality Design & Development (QD&D) Control and Assurance during Product Development Process (PDP) activities as well as continuation design & development support for sustaining manufacturing and product distribution.

Essential Functions:

  • Develop and execute Quality Plans for Quality Product Design and Development projects.
  • Collaborate with engineering teams to initiate and support the development and updates of Risk Management documentation in accordance with project requirements .
  • Establish severity and risk-based Process Master Validation Plan strategies with appropriate V&V rationales.
  • Support operational and process qualifications for customer manufacturing processes in collaboration with engineering teams.
  • Drive Test Method development with Operational and Business considerations and execution of Test Method Validations to measure effectiveness.
  • Implement inspection plans for Incoming, In-Process and Final Product.
  • Develop and justify appropriate sampling plans with characterization of test and inspection methods.
  • Represent Quality Engineering in design reviews.
  • Support initial qualification audit activities for Customer and Regulatory Agencies.
  • Support qualification activities related to supplier and vendor design characterization requirements for projects, including conducting audits and assessments.
  • Support Quality Best Practices and contribute to continuous improvement in GDP/GMP.
  • Apply sound, systematic problem-solving methods in identifying, prioritizing, communicating, and resolving quality issues.
  • Ensure that all site personnel comply with the site-level Quality Management System and training requirements.
  • Support the development of Quality Agreements for external customers.
  • Adhere to the TOMZ Quality Management System.
  • Perform other duties as assigned.

Qualifications:

  • Advanced Post-Secondary Education, Training or Certification coursework.
  • Knowledge of statistical techniques to analyze process capability.
  • Quality certification(s) (e.g., ASQ CQE, QCI, etc.).
  • Skilled in First Article Inspections and Component Qualifications.
  • Knowledge and experience with external standards: ISO 900/9001, ISO 13485, and 21

    CFR 820, EU MDR, pertaining to product development, design controls, good manufacturing practices, supplier qualification, auditing, quality control (GD&T, Nonconforming Materials, MRB), Corrective and Preventive Actions, and customer complaints).
  • Experience in effectively supporting audits by customers and external regulatory agencies.
  • Strong verbal and written English language communication skills.
  • Successfully meet TOMZ-specific positional and functional on-the-job training requirements.
  • Proficiency with Microsoft Office.
  • A self-starter capable of working independently and as part of a team, with the ability to collaborate across various functional areas, including R&D, Manufacturing, and QA, to achieve results.

Education:

  • Minimum 4-Year degree or equivalent of directly transferrable industry work experience (Engineering or Quality discipline preferred).

Experience:

  • Minimum of 2-5 years’ experience in a regulated manufacturing environment.
  • Experience in Class I, II, and/or III medical device manufacturing within a regulated environment (e.g., Aerospace, Defense, Pharmaceutical, etc.).

Physical Requirements:

  • Ability to bend, stoop, squat, kneel, and lift up to 50 pounds. Team lift or mechanical assistance required for objects over 50 pounds.
  • Ability to sit for prolonged periods.
  • Exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp-edged materials. Personal protective equipment (PPE) such as safety glasses, dust masks, ear plugs, cut-resistant or chemical-resistant gloves, and engineering controls may be required.
  • Perform keyboard entries with frequent operation of a computer.
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