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Quality Systems Engineer Jobs in Michigan (NOW HIRING)

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Quality Engineer

Warren, MI · On-site

$85K - $110K/yr

They will establish product quality controls , process controls , and automotive quality systems at appropriate levels of production. After launch of new product, Quality Engineer becomes the primary ...

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Quality Engineer

Sterling Heights, MI · On-site

$85K - $110K/yr

They will establish product quality controls , process controls , and automotive quality systems at appropriate levels of production. After launch of new product, Quality Engineer becomes the primary ...

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Quality Engineer

Southfield, MI · On-site

$85K - $110K/yr

They will establish product quality controls , process controls , and automotive quality systems at appropriate levels of production. After launch of new product, Quality Engineer becomes the primary ...

Adient plc

Quality Engineer

Battle Creek, MI · On-site

$85 - $110/hr

Quality Systems & Continuous Improvement * Drive continuous improvement across key production ... Support Manufacturing Engineering in maintaining and updating Process Failure Mode and Effects ...

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Adient

Quality Engineer

Battle Creek, MI · On-site

$67K - $87K/yr

Key Responsibilities Quality Systems & Continuous Improvement * Drive continuous improvement across ... Support Manufacturing Engineering in maintaining and updating Process Failure Mode and Effects ...

Apolis

LabWare LIMS Systems Engineer

Kalamazoo, MI · On-site

LabWare LIMS Systems Engineer Location: Kalamazoo, MI (Onsite) Tax Term (W2, C2C): W2/C2C Job Type ... Familiarity with code quality and linting tools and a strong testing/automation mindset. Role and ...

BWT LLC

Quality Engineer

Coldwater, MI · On-site

$25 - $30/hr

Entry-Level Quality Engineer Bluewater Thermal Solutions Bluewater Thermal Solutions is seeking a ... quality systems, manufacturing processes, and continuous improvement. We are looking for a ...

Weiss-Aug MedPharma

Weiss-Aug, is a leading provider of advanced manufacturing and engineering solutions with advanced ... We're currently seeking a passionate and skilled Quality Systems Manager - Medical Device ...

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How much do quality systems engineer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for quality systems engineer in Michigan is $43.60, according to ZipRecruiter salary data. Most workers in this role earn between $33.51 and $47.16 per hour, depending on experience, location, and employer.

What is a quality systems engineer?

Quality Systems Engineers are professionals responsible for designing, implementing, and maintaining quality management systems within an organization. They ensure that products or services meet established standards and regulatory requirements by developing processes, conducting audits, and analyzing data to identify areas for improvement. Their role often involves collaborating with other departments, training staff on quality procedures, and ensuring compliance with industry certifications such as ISO 9001. By maintaining effective quality systems, they help organizations deliver consistent, high-quality outcomes and reduce the risk of defects or non-conformance.

What does a quality systems engineer do?

A quality systems engineer conducts frequent and detailed quality checks to make sure the products and processes in a manufacturing setting are consistent and meet both industry and client standards as well as legal demands. In this role, you may monitor processes in various industries, so job duties can vary. However, you always play a role in locating and fixing defects. You check tools and materials, conduct tests, and train employees to meet safety requirements. You also closely document any problems for the engineer, who finds a solution. You follow the entire manufacturing process from beginning to end. In this job, you may work in a lab or an office.

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

To thrive as a Quality Systems Engineer, you need a solid background in quality management principles, process improvement methodologies, and a degree in engineering or a related field. Familiarity with ISO standards, Six Sigma or Lean certifications, and experience with quality management systems (QMS) software are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you excel in cross-functional teams and drive quality initiatives. These competencies ensure compliance, continuous improvement, and the delivery of high-quality products or services.

How does a quality systems engineer typically collaborate with cross-functional teams within an organization?

Quality Systems Engineers often work closely with various departments such as production, engineering, regulatory affairs, and supply chain to ensure that quality management systems are effectively implemented and maintained. They facilitate communication among teams to address compliance issues, resolve process deviations, and implement continuous improvement initiatives. Regular meetings, audits, and training sessions are common ways they collaborate to uphold quality standards and meet regulatory requirements. This collaborative approach helps ensure that quality objectives are integrated throughout all stages of the product lifecycle.

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

AspectQuality Systems EngineerQuality Assurance Engineer
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentManufacturing, aerospace, automotive, medical devicesManufacturing, software, healthcare, consumer products
ResponsibilitiesDeveloping and maintaining quality management systems, ensuring compliance, process improvementTesting products, identifying defects, ensuring product quality before release

While both roles focus on quality, the Quality Systems Engineer primarily develops and maintains quality management systems and processes, ensuring compliance across the organization. The Quality Assurance Engineer concentrates on testing products and identifying defects to ensure product quality before reaching customers. Both roles often collaborate but serve different stages of the quality management lifecycle.

More about Quality Systems Engineer jobs

What are the most commonly searched types of Quality Systems Engineer jobs in Michigan?

The most popular types of Quality Systems Engineer jobs in Michigan are:

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For Quality Systems Engineer jobs in Michigan, the most frequently searched job titles are:

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The top searched job categories for Quality Systems Engineer jobs in Michigan are:

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For Quality Systems Engineer jobs in MI, the most frequently searched job titles are:

Quality Systems Engineer jobs near you
Infographic showing various Quality Systems Engineer job openings in Michigan as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,697 per year, or $43.6 per hour.

Senior Quality Systems Specialist

Niowave Inc.

Lansing, MI

$75K - $103K/yr

Full-time

Re-posted 27 days ago

Job description

Senior Quality Systems Specialist
Who we are…
We are a team of scientists, engineers, technicians, and innovators dedicated to changing the world by developing medical isotopes to treat and eradicate cancer. We believe in building an environment where collaboration, curiosity, and camaraderie thrive. We also enjoy darts, cornhole, ping-pong, chili cook-offs, and other fun events that makes our company a community where we make a life, not just a living.
Who you are…
You are someone who genuinely cares about doing things the right way and finds purpose in work that requires integrity, structure, and trust. Quality and compliance resonate with you because you enjoy bringing clarity to complexity and creating systems that people can rely on. You are naturally collaborative and value building strong relationships, listening to different perspectives, and helping teams align in practical and meaningful ways. You take pride in being dependable and thoughtful, approaching challenges with sound judgment and a steady, solutions-oriented mindset. You are motivated by continuous improvement and enjoy helping others learn, grow, and succeed. Words that describe you include thoughtful, collaborative, principled, dependable, and grounded.
What you can expect to work on…
The Senior Specialist is a highly experienced subject matter expert who leads strategic Quality Systems initiatives, supports audit and inspection strategy, and influences organizational compliance direction. This role serves as a key advisor across functions, mentors team members, and drives continuous improvement and regulatory excellence. This role serves as a trusted collaborator to leadership, assists in guiding team direction, and leads efforts in high-visibility regulatory environments.
  • Leads, configures, and optimizes QS software systems, ensuring proper workflows, validations, and integrations for deviations, CAPAs, change control, and document control modules
  • Serves as the site-level subject matter expert for regulatory inspections and audits
  • Serves as the primary implementer for resolutions to audit and inspection findings, including:
    • Document revisions and creation of SOPs and QS procedures
    • Updating forms, templates, and training materials
    • Ensuring proper execution of CAPAs arising from audits
  • Leads or supports front room and backroom audit activities, ensuring timely and compliant responses; Implements and maintains a robust audit program
  • Conducts complex investigations, root cause analyses, and effectiveness checks
  • Mentors and coaches Quality Systems Specialists and technical staff to develop capabilities across the organization
  • Leads cross-functional initiatives, influencing stakeholders and building consensus on quality-related decisions
  • Drives enterprise-level continuous improvement and system optimization
What you need to succeed…
  • Bachelor’s degree in Life Sciences (biology, chemistry, biochemistry, Engineering (chemical, biomedical, industrial), or related field
  • 10+ years of GMP/Quality experience in pharmaceutical or biotech environments
  • Demonstrated experience with the following:
    • Managing complex quality systems, regulatory audits, and QS software implementations
    • Configuring and optimizing QS software systems, ensuring compliance and efficiency
    • Advanced proficiency in Microsoft Office, including Word, Excel, PowerPoint, and Outlook, with the ability to create professional documents, presentations, and reports, and efficiently manage communication and workflow across the organization
    • Mentoring/coaching quality team members
  • Embraces and models the Niowave Core Values of Teamwork, Courage, Integrity, and Upright Zeal
  • Develops and maintains good relationships, gains the confidence of others, and works effectively in a multidisciplinary matrix environment
    • Understands how to integrate into a new team/organization
      • Appreciates the current state of systems and processes and exercises sound judgment in proposing and implementing improvements
    • Understands personal communication and learning styles and adapts approach to connect effectively with others
  • Displays excellent interpersonal, written, and oral communication skills
  • Possesses strong organizational and project management skills for self and teams
  • Possesses a strong interest and ability to coach and mentor staff members and teams
  • Demonstrates strategic thinking with creative and excellent problem solving, root cause investigation, and decision-making skills with ability to critically interpret and use data to manage risk
  • Possesses advanced understanding of GMP regulations (FDA, EMA, ICH) and QS principles
Great to have…
  • Master’s degree in Life Sciences, Engineering, or related field
  • 12+ years of GMP/Quality experience in pharmaceutical or biotech environments
  • Professional certifications (e.g., ASQ Certified Quality Auditor, Six Sigma, Lean)
  • Experience with the following:
    • Leading or supporting regulatory inspections (FDA, EMA)
    • Implementing QS software systems, resolving audit findings, and creating training programs
    • Working in a facility with radiation regulatory requirements
Other things to know…
  • Full-time position
  • The company’s standard operating hours are Monday thru Friday 6:00 a.m. – 6:00 p.m. with production related activities requiring 24/7/365 shifts
  • This position will have regular working hours Monday - Friday within the standard operating hours
  • There is an expectation of adjusting working hours outside the standard hours to meet operational requirements as needed
  • Niowave has multiple locations within the Lansing area and travel between locations is expected in the role
Please provide a cover letter specifically describing the nature of your background and experience as it relates to this position.

Apply