Top 13 Qc inspector Jobs in Earth City, Mo

Quality Control (QC) Supervisor
Allied Medical, LLC —Earth City, MO
- $57,000 - $67,000 a year
- Full-time
- Computer literacy
- 3 years
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
QC Floor Inspector
Allied Medical LLC —Earth City, MO
- Mid-level
Quick Apply
QC Inspector
Anodyne Surgical —O'Fallon, MO
- $20 - $25 an hour
- Overtime
- Surgery
- Computer literacy
- Basic math
- Paid holidays
- Health insurance
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Instrumentation & Controls Inspector - Water - St. Louis
Black & Veatch Family of Companies —Creve Coeur, MO
- Full-time
- Background check
- Construction site
- Pass drug screening
- Wellness program
- AD&D insurance
Quality Control (QC) Supervisor
Allied Medical LLC —Earth City, MO
- 3 years
- Mentoring
- US work authorization
Quick Apply
Authorized Inspector Trainee - St Louis, MO
Bureau Veritas —St. Louis, MO
- Full-time
- Computer literacy
- Basic math
- High school diploma or GED
Traveling Quality Inspector
icon Mechanical —Granite City, IL
- 10 hour shift
- Construction site
- Mid-level
- 3 years
- Paid parental leave
- Paid holidays
Quick Apply
Quality Control Inspector
Walker Products Inc. —Pacific, MO
- $20 - $23 an hour
- Full-time
- Background check
- Mid-level
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Quality Control Inspector
Semco —St. Louis, MO
- $20.50 - $22.50 an hour
- 8 hour shift
- Computer literacy
- ERP systems
- Ability to lift 50 pounds
- Mileage reimbursement
Quick Apply

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QC Floor Inspector
Allied Medical LLC —Earth City, MO
Proven ability to read and interpret detailed engineering blueprints and technical drawings. You own the quality of every part you approve.
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Quality Control (QC) Supervisor

Allied Medical, LLC -
Earth City, MO

Quick Apply

Job Details

Full-time
$57,000 - $67,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Mechanical blueprint interpretation
Measurement-based inspection
Computer operation
Staff supervision
Teamwork
Blueprint specification interpretation
Team leadership
Test equipment calibration
ISO standards
GMP
Laboratory equipment calibration
Bachelor's degree
Quality risk management
Continuous improvement
Blueprint reading
Organizational skills
Product audits
Computer skills
Quality audits
Defect tracking tools
Regulatory compliance analysis
Project leadership
Non-conformance reporting

Full Job Description

Position Summary Main Job Functions

Note: In addition to these functions, employees are required to carry out such other duties as may reasonably be required.

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.

Supervisory Responsibilities/Position in Structure
Attach outline organization chart, as appropriate.

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

Main Duties
Duties/responsibilities (in order of priority)

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

Experience Required

ESSENTIAL

· 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.

DESIRABLE

· 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

ESSENTIAL

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

DESIRABLE

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

Pay: $57,000.00 - $67,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Experience:

gauge: 3 years (Required)
Blueprint reading: 3 years (Required)

Work Location: In person

Quick Apply

Refine Your Search

qc inspector jobs in earth city, mo

Quality Control (QC) Supervisor

QC Floor Inspector

QC Inspector

Instrumentation & Controls Inspector - Water - St. Louis

Quality Control (QC) Supervisor

Authorized Inspector Trainee - St Louis, MO

Traveling Quality Inspector

Quality Control Inspector

Quality Control Inspector

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