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Senior Quality Engineer

STERIS · St. Louis, MO

Apply on STERIS ↗
Level
Senior
Team
Quality
Base pay
$93k–$120k
Degree
Required
Experience asked
5+ years
Industry
Medical devices
Posted
5 days ago

The role in 30 seconds

A senior quality role at STERIS (medical devices) in St. Louis, MO. Louis, Missouri facility is responsible for managing processes and leading projects to maintain and improve the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP and FDA 21 CFR Part.

They ask for
5+ years · degree required
Tools it names
SPC, CAPA, ISO 13485, FDA / GMP, Supplier quality
Base pay
$93k–$120k
Day to day
some off-shift / weekend coverage

Read from the posting. The full description is below.

From the plant jobs report · week of November 2, 2026

Quality Engineer roles in Missouri: typical posted base $93k–$136k. This one lists $93k–$120k.

Median of the low and high ends of 11 live postings that list pay, out of 24 quality engineer openings in Missouri, read from manufacturers' own careers sites.

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

How this role compares

Against 23 other live quality postings in Missouri.

Base pay
About 10% below similar roles

Typical $100k–$136k, from 10 postings that list pay.

Experience asked
Typical (5+ years)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • Root cause 63%
  • Six Sigma 63%
  • Lean 38%
  • ✓ SPC 33%
  • ✓ CAPA 33%
  • FMEA 33%

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

It asks for 5+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Off-shift / weekend coveragePromotion path mentioned

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 STERIS

    We found 1 person at this company and state: 1 leaders, plus 1 likely hiring manager. 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 Mike → (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 does off-shift and weekend coverage work?
    • 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: STERIS in St. Louis

4 other open roles at this site · 1 person we found in quality roles at STERIS.

Senior Quality Engineer at STERIS in other locations

STERIS lists this title in 2 places. Pick the plant you can get to.

Full description from STERISAs posted on their careers site.Show

Position Summary

The Senior Quality Engineer in our St. Louis, Missouri facility is responsible for managing processes and leading projects to maintain and improve the quality system in accordance with the

requirements

of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP and FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role leads complaint/CAPA investigations, supplier quality improvement actions, operations production and process control improvements, and product and service quality improvements with the use of statistical techniques and other accepted quality principles. This role plans and executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems.

This position requires working onsite in our St. Louis, Missouri facility Monday through Friday 7:00am to 4:30pm. Must be able to respond to after hours calls per business needs.

What You'll do as a Senior Quality Engineer

  • ◆Serves as the Core Team Member on cross-functional new product/service development teams with focus on the execution of quality plans and design/service transfer.
  • ◆Develops and implements statistically valid sampling plans, designed experiments, capability studies, SPC and trend analysis in support of products and service improvements.
  • ◆Leads process and product corrective actions and problem-solving activities.
  • ◆Reviews the current quality system and recommend / implement improvements as needed.
  • ◆Uses data to perform statistical analysis and recommend process / product changes to improve product and service quality.
  • ◆Leads projects focused on quality system, product quality and service quality improvements.
  • ◆Develops analyses and reports on the performance of the quality system.
  • ◆Leads supplier audits and corrective actions.
  • ◆Leads and supports internal and external quality system audits.
  • ◆Instructs other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
  • ◆Collaborates with other departments and facilities within the company on quality related issues.
  • ◆Supervises Quality Engineers and other Quality staff in the execution of their assigned duties and objectives.
  • ◆Maintains product integrity and quality through the evaluation and disposition of nonconforming materials and processes.
  • ◆Perform all other duties as assigned.

Required

  • ✓Bachelor’s degree in Engineer, preferably Chemical Engineering, Biochemical Engineering, or Biomolecular Engineering.
  • ✓Minimum of 5 years of related experience (Manufacturing/Quality Engineering and/or Quality Systems experience).
  • ✓Minimum of 5 years of experience working in an ISO certified environment required
Show full description ↓

Preferred

  • +Experience with medical device, pharmaceutical or other regulated industries preferred.
  • +Experience with statistical analysis software and Visio preferred.
  • +ASQ, QMSR or familiarity with QMSR/GMP regulations preferred.

Other

  • •Ability to think critically and prioritize tasks, keeping the impact to the Customer at the forefront.
  • •Balance, manage, and execute continuously changing priorities, while collaborating with Production.
  • •Excellent problem-solving skills.
  • •Focus on identification of potential issues and continuous improvement.
  • •Experience working on cross-functional teams and on own initiative.
  • •Demonstrated excellent organizational, oral and written communications skills.

What STERIS Offers

We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future.

Here is just a brief overview of what we offer

  • •Market Competitive pay
  • •Extensive Paid Time Off and added Holidays
  • •Excellent Healthcare, Dental and Vision benefits
  • •Long- and Short-Term Disability coverage
  • •401(k) with a company match
  • •Maternity and Paternity Leave
  • •Additional add- on benefits / discounts for programs such as Pet Insurance
  • •Tuition Reimbursement and continuing education programs
  • •Excellent opportunities for advancement in a stable long-term career

Pay range for this opportunity is $92,650.00 - $119,900.00. This position is eligible for bonus participation.

Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.

STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits

Open until position is filled.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com .

If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.

The full affirmative action

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