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Quality Oversight Engineer Jobs in Wisconsin (NOW HIRING)

Quality Manager

Milwaukee, WI · On-site

$75K - $85K/yr

At a minimum, an associate's degree in an engineering discipline is preferred . 5 -7 years of ... Oversight of Sample Tracking System - New and Existing * Hold or Release product * Tooling Issues:

Solar Quality Control Manager

Waukesha, WI · On-site

$83K - $111K/yr

... engineering and construction solutions for solar, Walbec is your bridge to expertise in ... Construction & Field Quality Oversight * Perform routine field audits and inspections to ensure ...

WI · On-site

$93 - $124/hr

Provide quality oversight for mechanical, electrical, plumbing, fire protection, controls, and ... Education: BS in Construction Management, Engineering, QS, Architecture, or related fieldExperience ...

New

WI · On-site

$142 - $213/hr

... engineering, product, and operations teams -- ensuring that products spanning consumer health ... Develops and advances quality oversight frameworks for AI/ML and generative AI products, including ...

WI · On-site

$79 - $158/hr

The Quality Engineer ensures the quality of products and processes at a Carrier manufacturing ... oversight by people. #J-18808-Ljbffr

New

Showing results 21-40

Quality Oversight Engineer information

What is a quality oversight engineer?

Quality Oversight Engineers are professionals responsible for ensuring that products, processes, and systems meet established quality standards and regulatory requirements. They monitor manufacturing or production operations, conduct audits, and collaborate with various teams to identify and resolve quality issues. Their role often includes reviewing documentation, implementing corrective actions, and ensuring compliance with industry regulations to maintain high-quality outputs. Additionally, they may provide training and guidance to staff on quality best practices and assist in continuous improvement initiatives.

How does a quality oversight engineer typically collaborate with cross-functional teams to ensure compliance and product quality?

Quality Oversight Engineers work closely with production, engineering, and regulatory teams to monitor processes and ensure adherence to quality standards. They often participate in project meetings, conduct audits, and review documentation to identify potential risks or non-conformities. Effective communication and teamwork are essential, as these engineers provide feedback, recommend corrective actions, and help implement process improvements. This collaborative environment helps maintain high product quality and regulatory compliance throughout the manufacturing lifecycle.

What are the key skills and qualifications needed to thrive as a quality oversight engineer, and why are they important?

To thrive as a Quality Oversight Engineer, you need a solid background in quality management, engineering principles, and regulatory compliance, often supported by a degree in engineering or a related field. Familiarity with quality management systems (QMS), ISO standards, root cause analysis tools, and certifications such as Six Sigma or ASQ CQE are common requirements. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills to excel in this role. These competencies ensure that products and processes consistently meet standards, mitigate risks, and support organizational excellence.

What is the difference between Quality Oversight Engineer vs Quality Assurance Engineer?

AspectQuality Oversight EngineerQuality Assurance Engineer
CertificationsISO, Six Sigma, ASQ certifications often preferredISO, Six Sigma, ASQ certifications often preferred
Work EnvironmentRegulated industries like pharmaceuticals, medical devices, manufacturingSoftware, manufacturing, service industries
Primary FocusOverseeing compliance, audits, and quality systemsDeveloping and executing testing plans, process improvements
Employer UsageManufacturers, biotech, pharma companiesTech companies, manufacturing, software firms

While both roles focus on quality, the Quality Oversight Engineer primarily ensures compliance and oversees quality systems, often in regulated industries. The Quality Assurance Engineer concentrates on testing, process improvements, and preventing defects during product development. Understanding these differences helps candidates target the right roles based on their skills and industry focus.

Are quality oversight engineers paid well?

Quality oversight engineers typically earn competitive salaries that reflect their expertise in quality assurance, compliance, and process improvement. Compensation varies based on experience, industry, and location, but they generally receive benefits and opportunities for advancement in manufacturing, aerospace, or healthcare sectors.

Is a Quality Oversight Engineer a good career?

A Quality Oversight Engineer is a valuable role focused on ensuring product and process quality through inspections, audits, and compliance with standards. It often requires knowledge of quality management systems, industry regulations, and relevant certifications, making it a stable career with opportunities for advancement in manufacturing, healthcare, or technology sectors.

What are popular job titles related to Quality Oversight Engineer jobs in Wisconsin?

For Quality Oversight Engineer jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Quality Oversight Engineer jobs in Wisconsin look for?

The top searched job categories for Quality Oversight Engineer jobs in Wisconsin are:

What cities in Wisconsin are hiring for Quality Oversight Engineer jobs?

Cities in Wisconsin with the most Quality Oversight Engineer job openings:

Infographic showing various Quality Oversight Engineer job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Design Quality Assurance Manager

Agiliti Health, Inc

Milwaukee, WI • On-site

$120 - $190/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago


Agiliti rating

7.5

Company rating: 7.5 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

128th of 281 rated repair and maintenance companies


Job description

POSITION SUMMARY

The Design Quality Assurance Manager provides quality leadership and oversight for medical device design and development activities to ensure compliance with applicable regulatory and quality system requirements. This role partners closely with R&D and cross-functional teams to embed quality, risk management, and patient safety throughout the product lifecycle. This role will require 30% travel.

PRIMARY OBJECTIVES AND RESPONSIBILITIES
  • Lead quality oversight for new product development, ensuring compliance with 21 CFR 820.30, ISO 13485, MDSAP, and applicable global regulations.
  • Partner with R&D to ensure effective execution of design controls, including design planning, inputs, reviews, verification, validation, transfer, and maintenance of Design History Files (DHF).
  • Review and approve design and development documentation to ensure accuracy, completeness, and alignment with regulatory and internal quality requirements.
  • Own and govern the risk management process in accordance with ISO 14971, including hazard analysis, FMEA, usability risk, and implementation of risk controls.
  • Provide technical leadership in design-for-quality, reliability engineering, human factors engineering, and test method development.
  • Ensure design changes follow robust change control processes, including impact assessments and timely updates to documentation.
  • Serve as subject matter expert for design controls and risk management during internal and external audits and regulatory inspections.
  • Lead, coach, and mentor Design Quality Engineers while fostering strong cross-functional collaboration and a culture of proactive quality and continuous improvement.
QUALIFICATIONS
  • Bachelor’s degree in Engineering (Mechanical, Biomedical, Electrical, Chemical, or related discipline) required.
  • Advanced degree preferred.
  • 5–10 years of experience in medical device quality assurance, quality engineering, or regulatory compliance for FDA Class I and II devices.
  • Minimum of 3 years of experience in a Senior or Principal Design Quality role with direct or indirect supervisory responsibility.
  • At least 1 year of CAPA ownership experience within a design and development environment.
  • Demonstrated expertise in design controls, product development processes, software‑embedded medical devices, and risk management.
  • Experience working in regulated environments governed by FDA QSR, ISO 13485, MDSAP, and ISO 14971.
  • Working knowledge of applicable standards such as IEC 60601, IEC 62366, IEC 62304, and EU MDR.
KNOWLEDGE, SKILLS, AND ABILITIES
  • Apply expert knowledge of medical device design controls and quality system regulations to guide compliant product development.
  • Analyze technical and quality data to support sound risk‑based and evidence‑driven decisions.
  • Communicate complex quality and regulatory requirements clearly to technical and non‑technical stakeholders.
  • Lead and develop high‑performing quality teams through coaching, mentoring, and performance feedback.
  • Collaborate effectively across R&D, Manufacturing, Operations, and Supplier Quality to achieve shared objectives.
  • Influence cross‑functional teams to proactively identify risks and implement effective mitigations.
  • Demonstrate strong organizational skills to manage multiple priorities in a fast‑paced development environment.
  • Champion a culture of continuous improvement, accountability, and patient safety.
DISCLAIMER

This job description in no way states or implies that these are the only duties to be performed by the employee in this position. It is not intended to give all details or a step‑by‑step account of the way each procedure or task is performed. The incumbent is expected to perform other duties necessary for the effective operation of the department and the company.

It is the policy of Agiliti to provide equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender identity, sex, sexual orientation, national origin, age, physical or mental disability, genetic information, marital status, status as a veteran, military service, or any other characteristic protected by applicable federal, state, or local civil rights laws. In addition, Agiliti will provide reasonable accommodations for qualified individuals with disabilities.

Agiliti strictly prohibits any form of retaliation against individuals who make good faith reports of alleged violations of this policy or who cooperate in Agiliti’s investigation of such reports.

Affinity Action Policy Statements

You may be required to obtain certain vaccinations, or provide proof of current vaccination status, based on customer and/or company requirements. If vaccination is required, Agiliti will provide specific directions and cover the expense at a participating clinic. Please note, this includes the COVID-19 vaccination.

  • Agiliti offers a robust suite of benefits for regular, full‑time, non‑union employees including: health insurance options for Medical, Dental & Vision plans, Short- and Long-Term Disability plans, Flexible Spending Accounts, Health Savings Accounts, Life Insurance Options, Paid Time Off, 401K Saving Plan with employer match, Employee Discounts, Tuition Reimbursement, Daily Pay program, Employee Assistance Program, and wellness programs.

Agiliti is an equal opportunity employer and provides reasonable accommodations to employees and applicants consistent with state and federal law.

Primary Job Location: Milwaukee Design Center Additional Locations (if applicable):

Job Title: Design Quality Assurance Manager

Company: Agiliti

Location City: Wauwatosa

Location State: Wisconsin

Agiliti helps hospitals reclaim millions of dollars in wasted spending by connecting broken medical equipment processes. Our Equipment Value Management (EVM) framework connects previously siloed departments with highly agile and fully integrated equipment workflows. Our customers also deploy the individual elements of EVM — Clinical Engineering, Onsite Equipment Management and Rental Services — to ensure patient‑ready equipment is in the right place at the right time. More than 7,000 hospitals and health systems rely on Agiliti to reduce costs and free their clinicians to spend more time caring for patients. Our nationwide network ensures quick response to customer needs throughout the U.S. We believe every interaction has the power to change a life. Join Agiliti and help make a difference for health care providers and patients nationwide.

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