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Quality Control Associate Jobs in Florissant, MO

Valcom

Quality Control Inspector

Hazelwood, MO · On-site

$20 - $25/hr

Associate degree in technical field, plus two years of related experience in Quality Control, or combination of relevant education, experience, and training. * Proven and successful track record ...

Acro Blue

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Quality Control Technician I

Saint Peters, MO · On-site

$20/hr

Position Summary We are seeking a detail-oriented Quality Technician I to join our Distribution ... all our associates. We achieve this by developing and maintaining a cooperative working ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Florissant, MO

Quality Control Associate information

See Florissant, MO salary details

$10

$23

$35

How much do quality control associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for quality control associate in Florissant, MO is $23.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $28.61 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What cities near Florissant, MO are hiring for Quality Control Associate jobs? Cities near Florissant, MO with the most Quality Control Associate job openings:
Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Florissant, MO as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $48,845 per year, or $23.5 per hour.

Quality Control (QC) Supervisor

Allied Medical LLC

Earth City, MO • On-site

Full-time

Re-posted 19 days ago

Job description

Description:

The Quality Control Supervisor oversees the daily operations of the QC department to ensure all medical devices are inspected, tested, and documented in compliance with FDA 21 CFR Part 820, ISO 13485, and applicable regulatory requirements. This role provides leadership to QC inspectors, ensures adherence to quality standards, and works cross-functionally to support continuous improvement in manufacturing quality.


MUST HAVE METROLOGY AND BLUEPRINT EXPERIENCE.


This role will oversee a team of Quality Control Inspectors (Union roles).


Leadership & Oversight

  • Supervise, train, and mentor QC inspectors, ensuring consistent application of inspection and testing procedures.
  • Assign and monitor daily workloads, prioritizing tasks to meet production and shipping schedules.
  • Foster a culture of quality, compliance, and accountability within the team.

Quality Control Operations

  • Oversee inspection and testing of incoming materials, in-process components, and finished medical devices per established procedures and specifications.
  • Review and approve inspection records, test results, and Certificates of Conformance.
  • Establish Quality Inspection Plans and equipment needs to ensure proper process control is in place with Quality Assurance, Operations, and Engineering
  • Ensure proper use and calibration of QC equipment, including measurement tools and test instruments.
  • Support and lead efforts of Gage Repeatability and Reproducibility (Gage R&R) and Test Method Validation with manufacturing engineers
  • Maintain control of nonconforming materials, including segregation, documentation, and disposition per established processes. Manage Material Review Board process to ensure reject parts are dispositioned appropriately.
  • Drive Material Return process
  • Supporting complaint investigation with inspection, test, documentation and implementation of Corrective/Preventive Actions.

Compliance & Documentation

  • Ensure QC activities comply with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other applicable standards.
  • Generate and review quality records, inspection reports, and Device History Records (DHRs) for accuracy and completeness.
  • Support internal and external audits by providing documentation and participating in audit activities.

Continuous Improvement

  • Identify and report quality trends, defects, or process deviations to Quality and Manufacturing leadership.
  • Collaborate with Engineering, Manufacturing, and Supply Chain to resolve quality issues and improve processes.
  • Support Corrective and Preventive Actions (CAPA) and root cause investigations.

Skills, Qualifications, Competence Level Qualifications/education/Specialist Training required

ESSENTIAL

  • · Organization
  • · Strong written and verbal skills
  • · Collaboration skills
  • · QC process skills
  • · Computer knowledge and skills (Microsoft suite)
  • · Leadership
  • DESIRABLE
  • · eQMS skills
  • · Knowledge of ISO 13485, MDSAP, 21 CFR 820, MDR 2017/745
  • · Quality engineering (ASQ or similar Certifications)
  • · Experience in various inspection methods and equipment
Requirements:

Experience Required

REQUIRED

  • · Associates or Bachelors. Degree in an Engineering field is preferred (mechanical preferred).
  • · 3-5 years’ experience in regulated medical device industry highly preferred.
  • · Strong familiarity with calibration methods/standards, various gage use, and failed equipment risk analysis.
  • · Strong knowledge of global Quality System regulations related Good Manufacturing Practices. (ISO 13485, 9001, 17025)
  • · Legally authorized to work in the United States.

PREFERRED

  • · Professional certification(s) relevant to the position preferred (e.g., CQA, CQM, and/or CQE).
  • · Experience with electronic quality system documentation management and statistical tools such as GageTrak, MiniTab, Solidworks, CAD, PowerBI, Windchill, SAP, QPulse,etc.
  • · Excellent written and verbal communication skills.
  • · Project leadership skills.
  • · Experience with quality inspection processes and equipment
  • Knowledge of safety requirements and legal standards

Aptitude/Skill Required

REQUIRED

  • · Organization
  • · Strong written and verbal skills
  • · Collaboration skills
  • · Engineering process skills
  • · Computer knowledge and skills (Microsoft Suite, Solidworks, CAD, Minitab or similar)

PREFERRED

  • · eQMS skills
  • · Knowledge of ISO 13485, MDSAP, 21 CFR 820, MDR 2017/745
  • · Quality engineering (ASQ or similar Certifications)
  • · Statistical Analysis