Medical Device QA Inspector - Early Shift (Irvine)

Aerotek; Irvine (CA); On-site; USD 29,000 - 41,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

HSA

Transportation benefits

PTO

Job summary

Aerotek is hiring Medical Device Quality Inspectors in Irvine, CA. Join a leading medical device manufacturer to ensure life-changing devices meet strict quality standards.

Roles are on-site with first and second shifts, including overtime opportunities, contract-to-hire with competitive hourly pay. Responsibilities include inspecting materials and finished goods, reviewing production docs, and escalating quality concerns in a GMP environment.

Qualifications

• 1+ year of Quality Inspection, QA/QC, or Manufacturing experience preferred.
• Experience in medical device, pharmaceutical, aerospace, or regulated manufacturing is highly preferred.
• Strong attention to detail and documentation skills.
• Familiarity with GMP, SOPs, and quality procedures is a plus.
• Proficiency with Microsoft Office (Excel, Word, Outlook).
• Reliable, dependable and able to thrive in a team environment.

Responsibilities

• Inspect raw materials, labels, and finished products.
• Review manufacturing and production documentation.
• Identify, document, and escalate quality concerns.
• Perform inspections in a cleanroom environment.
• Ensure products meet GMP, regulatory, and company standards.
• Maintain accurate quality records and documentation.
• Collaborate with production, quality, and laboratory teams.

Skills

Quality Inspection

QA/QC

Manufacturing

GMP SOPs

MS Office

Attention to detail

Teamwork

Job description

Aerotek is hiring Medical Device Quality Inspectors in Irvine, CA. Join a leading medical device manufacturer to ensure life-changing devices meet strict quality standards.

Roles are on-site with first and second shifts, including overtime opportunities, contract-to-hire with competitive hourly pay. Responsibilities include inspecting materials and finished goods, reviewing production docs, and escalating quality concerns in a GMP environment.