Quality Engineering Technician

Quality Engineering Technician Job Description The Quality Engineering Technician serves as a key technical resource for complex nonconformance investigations, product quality concerns, and manufacturing quality issues in a regulated production environment. This role independently leads investigations, drives root cause and corrective action activities, coordinates large and complex sorting efforts, mentors other technicians, and collaborates closely with Quality Engineering and Manufacturing teams to reduce recurring defects and continuously improve quality processes and systems. Responsibilities

- Lead investigations of nonconforming components, assemblies, finished devices, and supplier-related quality issues, ensuring thorough analysis, accurate documentation, and appropriate disposition.
- Independently evaluate complex or ambiguous quality concerns using engineering drawings, specifications, manufacturing procedures, quality records, product history, traceability data, and inspection techniques.
- Author, review, and complete defect and nonconforming material reports (DMRs/NMRs), rework logs (RLs), CAPA-related documentation, and other quality records in accordance with established procedures.
- Lead root cause investigations by evaluating failure modes, identifying contributing factors, recommending corrective actions, and verifying effectiveness.
- Partner with Quality, Manufacturing, Supplier Quality, Purchasing, Operations, and Engineering teams to resolve quality issues, support troubleshooting efforts, and drive process improvements.
- Lead and coordinate product or material sorting activities, including defining inspection criteria, determining resource requirements, training participants, and communicating results.
- Serve as a technical quality resource by interpreting acceptance criteria, providing guidance on quality system requirements, and escalating issues requiring engineering judgment.
- Identify quality trends and recommend improvements to inspection methods, manufacturing processes, procedures, workmanship standards, and employee training programs.
- Mentor, train, and review the work of Quality Engineering Technicians and other employees to ensure accuracy, consistency, and compliance with quality standards.
- Use Epicor and other quality or manufacturing systems to conduct product history, traceability, and investigation activities.
- Support the development and revision of inspection instructions, investigation tools, quality procedures, and related documentation to improve consistency and effectiveness.
- Represent the technician team in cross-functional quality discussions and communicate investigation findings, recommendations, and quality concerns to key stakeholders.

Essential Skills

- Typically five or more years of experience in quality inspection, quality engineering support, medical device manufacturing, or a related regulated manufacturing environment.
- Demonstrated experience independently leading nonconformance investigations and root cause analysis activities.
- Advanced knowledge of nonconformance processes, inspection methods, and quality system requirements in a regulated manufacturing setting.
- Strong ability to interpret engineering drawings, specifications, assembly procedures, workmanship standards, and acceptance criteria.
- Advanced proficiency with measuring and inspection equipment used in production and quality control environments.
- Demonstrated ability to lead root cause investigations and support the implementation of effective corrective actions.
- Strong technical writing and documentation skills, including the ability to produce clear, concise, and complete quality records.
- Advanced experience using ERP, manufacturing, document control, and electronic quality systems, including Epicor or similar platforms.

Additional Skills & Qualifications

- Associate degree in quality, manufacturing, engineering technology, or a related technical field is preferred.
- Experience working within a medical device or similarly regulated manufacturing environment is highly beneficial.
- Strong troubleshooting skills and the ability to systematically identify and resolve complex quality issues.

Work Environment This position operates in a regulated manufacturing and quality environment that focuses on medical devices or similar products. The role follows normal first-shift hours, typically from 7:00 a.m. to 3:30 p.m. You will work closely with manufacturing, quality control, inspection, packaging, purchasing, and engineering teams, using ERP systems such as Epicor, electronic quality systems, document control tools, and a range of measuring and inspection equipment. The environment emphasizes adherence to documented procedures, workmanship standards, and quality system requirements, with a strong focus on product traceability, nonconformance management, and continuous improvement.
Job Type & Location
This is a Contract to Hire position based out of Saint Paul, MN.
Pay and Benefits
The pay range for this position is $30.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Saint Paul,MN.
Application Deadline
This position is anticipated to close on Oct 8, 2026. About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.

If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.