QC Inspector - SR

Marquee Staffing; Santa Rosa (CA); On-site; USD 33,000 - 36,000; Full time

Job summary

Marquee Staffing is seeking a temporary QC Inspector in Santa Rosa to support the Quality team. You will inspect components, subassemblies, and finished medical devices to ensure compliance with quality standards.

This role requires a High School Diploma, 1–5 years QC experience, experience with measurement instruments, and the ability to read procedures, drawings, and specifications. Work in a cleanroom and follow GDP, SOPs and document results.

Qualifications

• High School Diploma or equivalent required.
• 1–5 years in Quality Control, preferably in medical device manufacturing.
• Ability to read procedures, drawings and specifications.
• Experience with measurement instruments and inspection techniques.
• Strong documentation, communication and problem-solving skills.

Responsibilities

• Perform inspections, audits, functional testing, and quality checks.
• Review lot history records and Device History Records (DHR).
• Inspect components, subassemblies, finished products, and tools.
• Document inspection and testing results following GDP requirements.
• Identify quality issues and support corrective actions.
• Perform product rework as needed.
• Work in a cleanroom environment.
• Perform temperature and particle count monitoring.
• Complete ERP (QAD) and MES transactions.
• Follow SOPs, work instructions, and established quality procedures.

Skills

Reading procedures

Measurement instruments

Inspection techniques

Documentation

Problem-solving

Communication

Education

High School Diploma or equivalent

Job description

Position

QC Inspector

Location

Santa Rosa

Schedule

Monday – Thursday, 5:00 a.m. – 3:30 p.m.

Pay

$24.00 – $26.00/hr, depending on experience

About the Role

Temporary Quality Control Inspector supporting the Quality team with inspections of components, subassemblies, and finished medical devices to ensure compliance with quality standards and regulatory requirements.

Key Responsibilities

• Perform inspections, audits, functional testing, and quality checks
• Review lot history records and Device History Records (DHR)
• Inspect components, subassemblies, finished products, and tools
• Document inspection and testing results following GDP requirements
• Identify quality issues and support corrective actions
• Perform product rework as needed
• Work in a cleanroom environment
• Perform temperature and particle count monitoring
• Complete ERP (QAD) and MES transactions
• Follow SOPs, work instructions, and established quality procedures

Requirements

• High School Diploma or equivalent
• 1–5 years of Quality Control experience, preferably in medical device manufacturing
• Experience with measurement instruments and inspection techniques
• Ability to read technical procedures, drawings, and specifications
• Strong documentation, communication, and problem-solving skills
• Ability to work in a fast-paced, regulated manufacturing environment