Quality Assurance Final Inspector - 2nd Shift (PTO)

RibbitZ LLC

West Chester (Chester County)

On-site

USD 42,000 - 56,000

Full time

3 days ago
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Benefits offered by this job

15% Shift differential
100 Hours of PTO in Your First Year
401(k) with Employer Match
Health plans including no-cost HSA
Dental & Vision Coverage
Uniforms provided
Paid Holidays
EAP
Wellness Coach Program
Climate-Controlled facility
Career growth opportunities

Job summary

RibbitZ LLC is hiring a Quality Assurance Final Inspector for the 2nd shift to be the final check before parts are shipped. You will inspect precision‑machined medical device components, read blueprints, and verify conformance to customer specs in a regulated setting.

Ideal candidates have 1–2+ years QA experience, strong attention to detail, and familiarity with ISO 9001/13485 environments. Overtime and growth opportunities available at a climate‑controlled, manufacturing facility.

Qualifications

  • 1–2+ years of Quality Assurance experience in a regulated environment.
  • Blueprint reading experience is required to interpret inspection requirements.
  • Strong attention to detail and commitment to quality is essential.
  • ISO 9001 and/or ISO 13485 experience preferred.

Responsibilities

  • Perform final inspections on precision-machined medical device components.
  • Read and interpret blueprints and inspection requirements.
  • Detect scratches, burrs, nicks, and surface finish defects, often under magnification.
  • Verify compliance with customer specifications and quality standards.
  • Support calibration and traceability of inspection equipment.

Skills

Quality assurance experience
Blueprint reading
Detail oriented

Education

High School Diploma
Bachelor's Degree preferred

Tools

Calibration equipment

Job description

RibbitZ LLC is hiring a Quality Assurance Final Inspector for the 2nd shift to be the final check before parts are shipped. You will inspect precision‑machined medical device components, read blueprints, and verify conformance to customer specs in a regulated setting.

Ideal candidates have 1–2+ years QA experience, strong attention to detail, and familiarity with ISO 9001/13485 environments. Overtime and growth opportunities available at a climate‑controlled, manufacturing facility.

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