Open until filled
The role
The Quality Supervisor leads a team of Quality specialists, technicians or inspectors focused on incoming product/component inspection, final QC inspection/testing of products, complaint investigation, NCR investigation, or production floor quality support. The Quality Supervisor develops and manages work assignments, analyzes and trends Quality performance data and utilizes problem solving methods to improve processes and eliminate Quality issues.In addition, as a contributor to Quality System compliance, the Quality Supervisor supports the site to ensure the Quality System adheres to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other regulatory standards, as applicable.
Other
- Customer Focused: Demonstrates a “Customer first” mindset. Responds with a sense of urgency
- Teamwork: Collaborates with others. Works in a professional manner to support team actions
- Results: Effectively manages work tasks. Is detail oriented and strives for continuous improvement. Ability to analyze technical issues. Ability to cope with change and shifting priorities
- Communication: Constructs clear written communication. Keeps manager and co-workers informed
- Job Knowledge: PC experience and working familiarity of common desktop applications including Excel and Word
- Initiative/Leadership: Takes ownership of task and projects and seeks clarification if unsure of direction
- Ability to analyze and interpret data; utilize problem solving methodologies and drive process improvements
What you need
Required
- Bachelor’s Degree (Engineering/Scientific)
- Minimum 4 years of production Quality and/or Quality Management Systems experience
- Minimum 4 years of experience in healthcare, medical device or other regulated industry
- Minimum 2 years of experience leading a team and/or supervising employees
Preferrednice to have
- ASQ, QSR, or familiarity with QSR/GMP regulations preferred
What you'll do
What You’ll do as a Supervisor, Quality
- Lead and manage assigned Quality staff to ensure effective Customer complaint and CAPA management.
- Lead and manage assigned Quality staff to effectively execute site calibration and maintenance records; training records; DHR records and environmental control monitoring.
- Lead and manage assigned Quality staff to effectively execute QC inspection procedures and capture associated non conformances.
- Lead and manage assigned Quality staff to effectively investigate non conformances.
- Lead the team in providing effective production floor Quality support.
- Lead and manage assigned Quality staff in effectively managing nonconforming materials including proper disposition and recordkeeping.
- Establish individual and team objectives to attain key metric performance and ensure alignment to overall Quality strategy.
- Analyze and trend Quality data to identify and drive product/service and process improvements.
- Lead the Team’s talent development processes and knowledge development.
- Assume other duties as assigned.
Pay and benefits
$79,688 – $103,125 a year
Employer providedWhat STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.
Here is a brief overview of what we offer:
- Market competitive pay
- Extensive paid time off and (9) added holidays
- Excellent healthcare, dental, and vision benefits
- Long/short term disability coverage
- 401(K) with company match
- Maternity and parental leave
- Additional add on benefits/discounts for programs such as pet insurance
- Tuition reimbursement and continued educational programs
- Excellent opportunities for advancement in a stable long-term career
Pay range for this opportunity is $79,687.50 - $103,125.00. 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.
Paid time off and 9 added holidays
Healthcare, dental and vision benefits
Short/long term disability coverage
401(k) with company match
Maternity and parental leave
Tuition reimbursement
Where you'll work
Mentor, OHOn-siteOpen in Maps (opens in a new tab)
More jobs in Mentor, OHEqual opportunity, accessibility and legal noticesSTERIS's statements, word for word
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 40% below the US median for Quality Assurance roles at this level.
This roleEmployer provided
Manager roles in the US105 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $79,688 | — | $103,125 |
| All US (middle half) | $126,000 | $153,000 | $167,500 |
This role: STERIS's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not STERIS's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership13
- Quality systems and risk5
- Investigations and CAPA4
- GMP and compliance3
- Lab testing and methods2
- Documentation and SOPs2
- Regulatory submissions1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- European UnionEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- FDA and partnersMDSAP(official source, opens in a new tab)The Medical Device Single Audit Program
Company hiring pulse
STERIS on Regulatory Jobs
- 30
- Open roles
- 21
- Distinct roles
- 14
- Locations
By discipline
- Quality28 93%
- Regulatory2 7%
By level
- Associate & Specialist18 60%
- Senior & Principal7 23%
- Manager4 13%
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Quality Supervisor at STERIS
Open until filled. $80K–$103K a year, employer provided.