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Senior Design Quality Engineer (Mechanical)

Stryker · Portage, MI

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Level
Senior
Team
Quality
Base pay
$78k–$130k
Degree
Required
Experience asked
2+ years
Industry
Medical devices
Posted
Today

The role in 30 seconds

A senior quality role at Stryker (medical devices) in Portage, MI. In this role, you will independently execute and own quality engineering activities for defined mechanical workstreams within new product development and partner with cross-functional teams, including R&D, Operations, Manufacturing, Suppliers, Testing, and.

They ask for
2+ years · degree required
Tools it names
Six Sigma, Root cause, SPC, FMEA, PPAP, GD&T
Base pay
$78k–$130k

Read from the posting. The full description is below.

From the plant jobs report · week of October 19, 2026

Quality Engineer roles in Michigan: typical posted base $78k–$149k. This one lists $78k–$130k.

Median of the low and high ends of 19 live postings that list pay, out of 57 quality engineer openings in Michigan, read from manufacturers' own careers sites.

Michigan plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 56 other live quality postings in Michigan.

Base pay
About 14% below similar roles

Typical $86k–$154k, from 18 postings that list pay.

Experience asked
Less than usual (2+ vs 4+)

Similar roles usually ask 4+ years.

Skills these teams ask for most

  • ✓ Root cause 70%
  • ✓ FMEA 53%
  • ✓ PPAP 49%
  • ✓ SPC 46%
  • Control plans 44%
  • ✓ Six Sigma 40%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 2+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at Stryker

    We found 3 people at this company and state: 2 in this kind of role, 1 leaders. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to Ryan → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Stryker in Portage

4 other open roles at this site · 3 people we found in quality roles at Stryker.

Full description from StrykerAs posted on their careers site.Show

What you will do

  • ◆Partner with R&D to evaluate mechanical product designs against quality

requirements

for safety, effectiveness, reliability, manufacturability, and usability, and translate customer and market feedback into clear design and quality

requirements

for assigned workstreams.

  • ✓Own risk management deliverables for assigned new product development workstreams, including developing risk management plans and reports, facilitating risk reviews, and verifying the effectiveness of design and process risk controls.
  • ✓Execute and coordinate design quality activities for assigned workstreams across requirements, design reviews, drawings, specifications, inspection methods, design verification and validation, and change control to ensure objective evidence supports product acceptance.
  • ✓Develop and execute design verification and validation strategies and requirements, including usability activities; review protocols and results; and complete final reports with clear, statistically valid conclusions.
  • ✓Partner with Operations and suppliers to develop, evaluate and implement robust manufacturing process controls for assigned mechanical components and assemblies.
  • ✓Coordinate product design and quality transfers to internal and/or external manufacturing facilities, including PPAP planning, supplier communication, readiness reviews, and approval of quality documentation.
  • ✓Identify and document critical quality attributes within assigned workstreams using risk-based methods and ensure alignment with design outputs and process controls.
  • ✓Own PPAP execution for assigned components or suppliers. Communicate PPAP

requirements

to component suppliers, evaluate submission readiness, and approve PPAP documentation and results within the assigned scope.

  • ✓Support quality system maintenance and improvement by identifying procedural updates and implementing effective, sustainable solutions.

What you will need

  • ✓Bachelor’s Degree in Mechanical Engineering or a related engineering discipline.
  • ✓2+ years’ experience in quality, manufacturing, new product development, or engineering.
Show full description ↓

Stryker is hiring a S enior Design Quality Engineer (Mechanical) in Portage, Michigan, to support our Medical business. In this role, you will independently execute and own quality engineering activities for defined mechanical workstreams within new product development and partner with cross-functional teams, including R&D, Operations, Manufacturing, Suppliers, Testing, and Regulatory, throughout the development process. You will be responsible for quality activities within assigned products, components, or suppliers, including risk management, design verification and validation, process controls, design transfer, and post-market quality support through the change control process. You may also contribute to and coordinate quality improvement initiatives within your assigned scope.

Preferred

  • +Experience within the medical device or regulated manufacturing industry.
  • +Working knowledge of ISO 13485 and ISO 14971.
  • +Experience with statistical analysis, sampling plans, statistical process control, and Minitab.
  • +Applied knowledge of Advanced Quality tools such as Failure Modes and Effects Analysis (FMEA), GD&T, tolerance analysis, Root Cause Analysis, and Mistake Proofing/Poka-Yoke.
  • +Ability to read and interpret CAD models, engineering drawings, specifications, and inspection requirements.
  • +Knowledge of polymer materials/processes and performance considerations for medical device applications.
  • +Six Sigma certification or ASQ certification.

United States of America Pay Ranges

  • •USN : $77,700 - $129,500 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

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