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Quality Control Inspector (DAL)

Regal Staffing Services

Scotland

On-site

GBP 60,000 - 80,000

10 days ago

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Job summary

An established industry player is seeking a diligent Quality Control Inspector to ensure compliance with Good Manufacturing Practices and Good Laboratory Practices. In this role, you will be responsible for auditing documentation, reviewing production records, and conducting quality system audits. This position offers a structured schedule from Monday to Friday, providing a stable work environment where your contributions will directly impact product quality. If you have hands-on experience in a GMP-regulated setting and are looking to grow in a quality assurance role, this opportunity is perfect for you.

Qualifications

  • 6 months - 1 year of experience as a Quality Auditor/Inspector.
  • Proficiency in MS Office and strong English skills required.

Responsibilities

  • Ensure compliance with GMP and GLP in Quality Control and Production.
  • Audit documentation for accuracy and participate in quality investigations.

Skills

Quality Control

Good Manufacturing Practices (GMP)

Good Laboratory Practices (GLP)

Batch record keeping

English proficiency

Spanish proficiency

Education

Experience in GMP-regulated environment

Tools

MS Office

Job description

Regal Staffing Services now hiring a Quality Control Inspector located in the Midlothian, TX area.

To Apply or Inquire: Call (469) 310-5850 and ask for Nayeli or Juana.

Shifts & Pay:
  • Schedule: Monday - Friday, 4:30 AM - 3:30 PM
  • Pay Rate: $19.00 per hour
Responsibilities:
  • Ensure GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) compliance in Quality Control (Q.C.) and Production.
  • Review and approve production filling batch records.
  • Audit and verify documentation for accuracy and compliance.
  • Confirm correct components and batch setup on packaging lines.
  • Review data from mechanics, machine operators, and line leads for accuracy.
  • Place non-conforming compounded batches and finished goods into Quarantine status.
  • Report quality issues and participate in investigations.
  • Conduct daily housekeeping audits in production areas.
  • Assist in GMP training for employees.
  • Participate in Quality System audits.
  • Ensure all SOPs (Standard Operating Procedures) are followed on production lines.
Requirements:
  • 6 months - 1 year of hands-on experience as a Quality Auditor/Inspector in a GMP-regulated environment (pharmaceutical, biomedical, or medical device industry preferred).
  • Experience with batch record keeping, CAPA initiation, and deviation investigation.
  • Strong English reading, writing, and speaking skills (Spanish is a plus).
  • Proficiency in MS Office (Word, Excel, Access, PowerPoint) and email.
  • Ability to occasionally lift and/or move up to 10 lbs.
  • Stable work history.
  • Must pass a background check and drug screen.
How to Apply:
  • Apply online at www.applyregal.com (Select "Dallas" as your branch).
  • Questions? Call (469) 310-5850.
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