QUALITY INSPECTOR

Randstad USA; Florida; On-site; USD 43,000 - 46,000; Full time

Job summary

Randstad USA is seeking an on-site Quality Inspector in Florida to verify raw materials and finished devices using precision tools and blueprints. The role requires 2 years of quality experience in regulated industries and strict adherence to FDA/ISO 13485 standards.

The position offers a first shift, 8 AM–4 PM, with a climate-controlled facility and competitive pay. High School education is expected, and overtime is possible up to 6 hours weekly.

Qualifications

• High School diploma or equivalent required.
• 2 years of quality inspection experience in regulated industries.
• Familiarity with inspection tools like calipers, micrometers and blueprints.
• Understanding of FDA/ISO 13485 standards is preferred.

Responsibilities

• Perform visual, dimensional, and functional testing on materials and devices.
• Enforce cGMP and ISO 13485 protocols in sterile environments.
• Maintain audit-ready logs, DHR, and data tracking for FDA audits.
• Identify defective items, issue NCRs, and work with engineers to root-cause.
• Complete quality review and authorize final release for packaging.

Skills

Product Inspection

Quality Assurance

Quality Control

Inspection

Production Control

Blueprints

Education

High School

Job description

Job Overview

We are seeking an on-site Quality Inspector to verify raw materials and finished devices using calipers, micrometers, and blueprints. This role requires 1–3 years of quality experience in a regulated industry (medical device, aerospace, or pharma) and strict adherence to FDA/ISO 13485 standards.We offer competitive pay, great benefits, and a clean, climate-controlled facility—

Key Details

• salary: $43,000 - $46,000 per year
• shift: First
• work hours: 8 AM - 4 PM
• education: High School

Responsibilities

1.Perform Inspections:Conduct thorough visual, dimensional, and functional testing on incoming raw materials, sub-assemblies, and finished medical equipment using precision instruments to verify alignment with strict engineering specs.

2.Enforce Sterile Standards:Monitor and audit the cleanroom or assembly line environments to ensure continuous compliance with cGMP, ISO 13485 protocols, and standard operating procedures (SOPs).

3.Document and Track:Maintain immaculate, audit-ready inspection logs, device history records (DHR), and data tracking files to satisfy internal stakeholders and external FDA investigators.

4.Isolate Defective Goods:Identify, flag, and physically segregate defective items or raw materials; initiate formal Non‑Conformance Reports (NCR) and collaborate with production engineers to trace root causes.

5.Approve Final Release:Perform the definitive quality review on fully completed medical systems and devices, providing the authorization signatures required for packaging and market distribution.

Essential Functions

The essential functions of this role include:

• working up to 6 hrs of overtime per week

Skills

• Product Inspection
• Quality Assurance
• Quality Control
• Inspection
• Production Control
• Blueprints

Qualifications

• Years of experience: 2 years
• Experience level: Experienced

Equal Opportunity Employer

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Accommodation Information

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Benefits

• medical
• prescription
• dental
• vision
• AD&D
• life insurance offerings
• short-term disability
• a 401K plan (all benefits are based on eligibility)

Pay

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc.

Posting Duration

This posting is open for thirty (30) days.