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Quality System Engineer Jobs (NOW HIRING)

$78K - $148K/yr

Create Alert The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will ...

We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery ... Minimum 12 years of compliance, quality systems, or regulatory program experience, or equivalent ...

EHC is currently looking for a Quality System Engineer for a client in the Houston, TX area. Job Summary: Quality Systems Engineers are exposed to multiple facets of our dredging projects with ...

Maintain and recommend improvements to the Quality Management System (QMS) to ensure compliance ... Bachelor's degree in engineering, quality management, or related scientific discipline. American ...

Maintain and recommend improvements to the Quality Management System (QMS) to ensure compliance ... Bachelor's degree in engineering, quality management, or related scientific discipline. American ...

Contract or Direct Hire Systems Engineer Position Overview The Systems Engineer is responsible for ... We help clients get work done more efficiently and economically, without compromising quality.

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Quality System Engineer information

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How much do quality system engineer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for quality system engineer in the United States is $50.03, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $54.09 per hour, depending on experience, location, and employer.

What is a quality system engineer?

Quality System Engineers are professionals responsible for developing, implementing, and maintaining quality management systems within organizations. They ensure that products and processes meet established quality standards and regulatory requirements. Their duties often include auditing internal processes, analyzing data to identify areas for improvement, and collaborating with various departments to implement corrective actions. Quality System Engineers play a crucial role in ensuring continuous improvement and compliance with industry standards such as ISO 9001.

How does a quality system engineer typically collaborate with cross-functional teams to ensure compliance and continuous improvement?

Quality System Engineers often work closely with teams such as manufacturing, regulatory affairs, R&D, and supply chain to maintain and improve quality management systems. They facilitate audits, coordinate corrective and preventive actions (CAPA), and provide training on quality standards. Regular meetings and process reviews help ensure that all departments are aligned with compliance requirements and best practices. This collaborative approach not only supports regulatory compliance but also drives continuous improvement initiatives across the organization.

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

To thrive as a Quality System Engineer, you need expertise in quality management systems (QMS), process improvement, and a relevant engineering degree or certification such as Six Sigma or ISO 9001 auditor credentials. Familiarity with tools like root cause analysis software, statistical process control (SPC), and document management systems is typically required. Strong analytical thinking, problem-solving, and effective communication skills help you collaborate across departments and drive continuous improvement. These skills ensure compliance with standards, enhance product reliability, and support operational excellence within an organization.

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

AspectQuality System EngineerQuality Assurance Engineer
CertificationsISO 9001 Lead Auditor, ASQ CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentManufacturing, ISO compliance, process improvementProduct testing, process validation, defect prevention
Industry UsageManufacturing, aerospace, automotiveSoftware, electronics, manufacturing

Both roles focus on quality but differ in scope. The Quality System Engineer primarily develops and maintains quality management systems, ensuring compliance with standards like ISO 9001. The Quality Assurance Engineer concentrates on testing products and preventing defects during production. While overlapping in quality principles, their daily tasks and focus areas vary based on organizational needs.

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Infographic showing various Quality System Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $104,058 per year, or $50 per hour.

Quality System Engineer III

Maple Grove, MN • Hybrid

Boston Scientific
Medical Equipment and Supplies Manufacturing • 10K+ employees

Full-time

Posted 21 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

34th of 547 rated manufacturers


Job description

Recruiter: Spencer Gregory Hale

Quality System Engineer III

 

About the role:

The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level.  This role will support Audit Excellence at Maple Grove, specifically focusing on the Internal Audit program to ensure the compliance and effectiveness of the BSC Quality Management System against external regulations/standards and BSC procedures.

At Boston Scientific, we value collaboration and synergy.  This is a hybrid work mode position located in Maple Grove, MN with the expectation to be in the office at least 3 days per week.

Your responsibilities include:

  • Execute Internal Audits of the Maple Grove Site as assigned
    • Audits may include: Production, Design, Regulatory, Management Controls, and CAPA
    • Evaluate and document the compliance of assigned areas via: Tours, Interviews, Documentation and Record Review
    • Formulate and document nonconformities and opportunities for improvement
    • Understand procedures and evaluate compliance to applicable requirements
  • Lead Internal Audits
    • Collaborate cross-functionally with Audit Area Management for audit scheduling, execution, and initiation of audit nonconformities
    • Develop an Audit Plan, including scope, objectives, criteria, and planned schedule
    • Facilitate Audit Opening and Closing Meetings
    • Provide work directions to Audit Team
    • Complete Audit records, including Audit Report and Audit Trails
    • Communicate audit progress and results to Auditees and Leadership
  • Support and lead Internal Audit initiatives, continuous improvement opportunities, and/or projects
    • Coordinate activities, communicate progress, collaborate on key deliverables, and influence action.
    • Make pragmatic, risk-based decisions and provide input regarding how to apply requirements and best practices for processes compliance, efficiency, and effectivity.
  • Serve as a Quality System Expert resource as requested
    • Support External Audit readiness and execution, including performing production line walks and documentation review.
    • Partner cross-functionally to provide guidance on BSC’s Quality Management system and external regulations/standards.

Required Qualifications:

  • Bachelor's degree
  • Minimum of 3 years of relevant quality engineering experience in the medical device or pharmaceutical industry
  • Minimum of 1 year experience in a role that includes auditing
  • Understanding of regulations/standards applicable to BSC Quality Management (such as 21 CFR 820 and ISO 13485)
  • Conceptual, practical, and functional knowledge of quality principles, with a general understanding of related job functions
  • Strong verbal and written communication, including technical writing, and organizational skills
  • Detail oriented with the ability to analyze information quickly 
  • Able to use a risk-based approach for making quality and business decisions

Preferred Qualifications:

  • 3+ years of experience in audit execution (such as Internal Audits, Supplier Audits, or Regulatory Audits)
  • ASQ Certified Quality Auditor
  • Proactive, able to work independently with minimal supervision, as a team leader or member
  • Ability to collaborate and communicate with all levels of the organization
  • Continuous improvement mindset with a passion for Quality
  • Proven ability to influence without authority in a matrixed organization
  • Strong networking skills to foster collaborative relationships

Requisition ID: 633424 

Minimum Salary: $ 78300 

Maximum Salary: $ 148800 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


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About Boston Scientific

Sourced by ZipRecruiter

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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