Quality Control Inspector I-II - Arlington, TX

Quality Control Inspector I-II - Arlington, TX

Contract Type:

Full Time

Location:

Arlington

Industry:

Pharmaceuticals

Contact Name:

Amber Mitchell

Contact Phone:

Date Published:

24-Jul-2025

Quality Control Inspector I/II
Location: Arlington, TX
Schedule: 11am-7pm CST

A growing contract manufacturer located in Arlington, TX is seeking a Quality Control Inspector I/II to join its Quality team. This role will be responsible for a range of quality control activities including receiving, in-process, and final inspections, as well as label verification and documentation reviews. This opportunity is offered on a full-time and permanent basis, and offers an hourly rate of between $19-22/hr.

This position reports to the Quality Assurance Manager and plays a key part in ensuring all materials and finished goods meet internal quality standards and customer specifications.

Key Responsibilities

Primary Duties (approx. 90%)

  • Perform inspections of raw materials, in-process components, final products, and labeling to verify conformance to specifications.
  • Use standard inspection tools such as calipers, micrometers, rulers, and pin gauges.
  • Verify completeness and accuracy of production documentation in accordance with GDP principles.
  • Review work orders and ensure information is accurate and complete.
  • Record results, document nonconformances, and support the team in root cause identification.
  • Work independently while adhering to defined inspection protocols and quality procedures.

Qualifications

Required:

  • High school diploma or equivalent.
  • 2–3 years of hands-on quality inspection experience, ideally within a regulated manufacturing environment (medical device, aerospace, or lab setting).
  • Ability to interpret engineering drawings and follow SOPs/work instructions with minimal supervision.
  • Familiarity with quality tools and equipment such as calipers, rulers, and other precision instruments.
  • Proficiency in Microsoft Office; ability to work with ERP and quality management systems.
  • Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).

Preferred:

  • Bachelor’s degree in a technical field such as engineering or applied science.
  • Exposure to SPC, Six Sigma, or risk-based quality approaches (e.g., FMEA, IQ/OQ/PQ).
  • Experience with digital QMS platforms such as Arena, uniPoint, or TrackWise.
  • Background working in cleanroom or controlled environment manufacturing.

Please apply with an updated copy of your resume to be considered.

...

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