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New · posted Oct 28

Midmark · Medical Devices

Supervisor, Quality Control

  • Kansas City, KS
  • On-site
  • Full-time
  • Manager
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EmploymentFull-time
DeadlineOpen until filled

The role

The Quality Control Supervisor leads and conducts activities to improve and assure quality control over the manufacturing of products and components. Responsible for overseeing and leading the testing and inspection of products at various stages of production, compiling and evaluating quality and statistical data, and driving actions to maintain consistent, reliable products and processes.

What you need

EDUCATION and/or EXPERIENCE

Associate Degree in Manufacturing, Mechanical Engineering, Quality, or a related technical field, with 1-2 years of experience in a quality, manufacturing, or engineering role and/or equivalent experience. Experience working within an ISO 9001 or ISO 13485 quality management system is preferred.

COMPETENCY and/or SKILL

  • Oracle (ERP)

  • Minitab

What you'll do

ESSENTIAL/PRIMARY DUTIES

  • Responsible for ensuring quality control activities comply with established company procedures, customer requirements, product specifications, and applicable business requirements.

  • Daily involvement in making decisions and/or providing technical data for decisions that impact compliance with design specifications.

  • Develops, maintains, and improves site quality processes, procedures, and controls to support consistent product quality and continuous improvement.

  • Apply problem solving tools/skills to effectively investigate nonconformances.

  • Plans and conducts the analysis, inspection, design, test, and/or integration to assure the acceptance of products or components.

  • Adheres to sampling procedures and designs/develops forms and instructions for recording, evaluating and reporting reliable quality data.

  • Actively engaged in conducting Gage R&R studies and maintaining associated measurement system data.

  • Responsible for conducting calibration per schedule and the monitoring and recording of the data.

  • Ability to lead a team and peers.

  • Versailles site specific duties: 

    • Responsible to ensure that activities comply with all specified regulatory agencies (FDA, ISO, UL, CSA, etc.) 

    • Participates and/or leads internal audits or external audits.

SECONDARY DUTIES

  • Apply Midmark Production System (MPS) concepts to identify and eliminate non-value added tasks and/or activities in the various areas of responsibility.

  • Ability to understand documents related to engineering function.  Documentation includes, but not limited to, layout drawings, detail drawings, assembly drawings, Bill of Materials, Change Orders, product and component test specifications and design records.

  • Actively lead or participate as a member of cross-functional product and process teams to acquire detailed product, process, and user knowledge.

  • Perform statistical analysis of manufacturing and quality data; collect, interpret, develop SPC limits, organize results, and identify opportunities for improvement.

  • Ability to support process qualification, capability studies, and associated quality activities.

SUPERVISORY RESPONSIBILITIES

  • Leads and directs the work of other teammates and has full authority for personnel decisions.

Where you'll work

Kansas City, KSOn-siteOpen in Maps (opens in a new tab)

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Working conditions

While performing the duties of this job, the teammate is regularly required to see, talk, and hear. The teammate frequently is required to sit and use hands. The teammate is occasionally required to reach with hands and arms. The teammate must regularly lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.

Equal opportunity, accessibility and legal noticesMidmark's statements, word for word

ADDITIONAL INFORMATION

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the teammate. Other duties, responsibilities and activities may change or be assigned at any time with or without notice. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

Midmark Equal Employment Opportunity Employer – Minorities/Females/Disabled/Veterans

The physical demands described here are representative of those that must be met by a teammate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The work environment characteristics described here are representative of those a teammate encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the teammate is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually quiet.

Job intelligence

The context around this role

Live data · October 28, 2026

Salary intelligence

How the pay compares

Manager roles in the US28 roles publishing pay

Middle half $103,250 to $129,125, median $112,000
Annual base pay
Annual base payLowMedianHigh
All US$103,250$112,000$129,125

Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 341 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Midmark's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Quality Inspector · Quality Control Inspector

    $61K median192 open
  2. One step back

    Senior & Principal

    Often: Scientist, Quality Control · Senior Scientist, Quality Control

    $96K median88 open
  3. This role

    Manager

    Often: Supervisor, Quality Control · Manager, Quality Control

    $112K median36 open
  4. Next step

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $198K median25 open

Skills DNA

What this role leans on

How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 3 linesDocumentation and SOPs: 4 linesInvestigations and CAPA: 1 lineValidation and qualification: 1 lineQuality systems and risk: 2 linesData and digital systems: 1 lineCollaboration and leadership: 5 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsData systemsTeamwork
  • Collaboration and leadership5
  • GMP and compliance4
  • Documentation and SOPs4
  • Lab testing and methods3
  • Quality systems and risk2
  • Investigations and CAPA1
  • Validation and qualification1
  • 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.

Company hiring pulse

Midmark on Regulatory Jobs

6
Open roles
6
Distinct roles
2
Locations

By discipline

  • Quality6 100%

By level

  • Senior & Principal4 67%
  • Manager1 17%
  • Associate & Specialist1 17%
See all 6 Midmark roles

More roles at Midmark

All 6 Midmark roles

Similar Quality Control roles elsewhere

Supervisor, Quality Control at Midmark

Open until filled.

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