Quality Control Inspector ( Med Device)

Ultimate Staffing

Irvine (CA)

On-site

USD 28,929 - 37,195

Full time

14 days+

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Job summary

A leading company in the medical device sector is seeking a Quality Inspector to ensure regulatory compliance and product quality. In this role, you will conduct inspections, document findings, and collaborate on quality improvements. With a focus on precision and detail, you'll help maintain high standards within a fast-paced environment. Candidates should have experience in quality assurance along with familiarity in the use of inspection tools.

Qualifications

Minimum 2 years of QA or Inspection experience in a regulated environment.
GMP and GDP experience required.
Proficient in English reading and writing.

Responsibilities

Perform receiving and in-process inspections.
Interpret blueprints and complete First Article Inspections (FAIs).
Ensure compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).

Skills

Attention to detail

Good Documentation Practices

Quality assurance

Inspection tools

Education

High school diploma or equivalent

Tools

Keyence measurement system

Manufacturing software

Job description

1 day ago Be among the first 25 applicants

This range is provided by Ultimate Staffing. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$22.00/hr - $27.00/hr

Direct message the job poster from Ultimate Staffing

Business Solutions Director at Ultimate Staffing

Quality Inspector - Medical Device (QA & Inspection Focus)

Onsite - Irvine, CA
$21 - $27/hour
Shift: 6:00 AM - 2:30 PM (May shift to 7:00 AM - 3:30 PM)
Contract: 6-Month Contract with Possible Extension

Perform receiving and in-process inspections

Interpret blueprints, GD&T, and complete First Article Inspections (FAIs)

Use inspection tools: hand tools and Keyence measurement system

Identify and distinguish critical vs. non-critical dimensions

Understand and apply dimensional tolerances down to the thousandths

Conduct label inspections, document reviews, and issue Certificates of Conformance (COCs)

Ensure compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP)

Provide feedback on GDP corrections to site personnel

Follow established quality procedures and contribute to continuous improvement

Accurately document and report nonconformances in the QMS

Minimum 2 years of QA or Inspection experience in a regulated environment

GMP and GDP experience required

Medical device experience is a plus

Strong understanding of inspection tools, measuring systems (Keyence), and procedures

Proficient in English reading, writing, and verbal communication

High attention to detail and ability to follow written procedures

Comfortable working independently and as part of a team

Basic computer skills and familiarity with manufacturing software

High school diploma or equivalent preferred

Apply now if you're ready to contribute to a high-quality, fast-paced environment with a focus on precision and compliance.

All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county , to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Seniority level