Medical Device Quality Technician | GMP & ISO 13485

Advantage Technical; Acton (MA); On-site; USD 36,000 - 48,000; Full time

Benefits offered by this job

Medical, Dental, Vision, and Pet Ins.

401(k) Retirement Savings Plan

Employee Assistance Program (EAP)

Commuter/Parking Accounts

People Perks Program

Health Savings Account (HSA)

AD&D Insurance

Job summary

Advantage Technical is seeking a Quality Technician in Acton, MA to support the development of innovative medical devices. You will perform inspections, review drawings, and document results in a regulated environment.

The role requires hands-on quality experience, attention to detail, and the ability to maintain accurate records per GMP/ISO 13485. Load-bearing patient safety context with a collaborative team.

Qualifications

• High school diploma or equivalent.
• 3+ years of experience in quality, manufacturing, assembly, or production environments.
• Ability to read technical drawings and specifications.
• Experience in medical device, cleanroom, or regulated manufacturing environments preferred.
• Comfortable performing repetitive inspections and data entry.

Responsibilities

• Perform in-process and final inspections on components and assemblies.
• Review engineering drawings, specifications, and quality documentation.
• Document inspection results, deviations, and non-conformances.
• Maintain accurate records in compliance with GMP and ISO 13485 standards.
• Support investigations, root cause analysis, and corrective actions.
• Collaborate with engineering and manufacturing teams to resolve quality issues.
• Follow cleanroom procedures and quality control requirements.

Skills

Quality inspection

Documentation

Reading drawings

Education

High school diploma or equivalent

Job description

Advantage Technical is seeking a Quality Technician in Acton, MA to support the development of innovative medical devices. You will perform inspections, review drawings, and document results in a regulated environment.

The role requires hands-on quality experience, attention to detail, and the ability to maintain accurate records per GMP/ISO 13485. Load-bearing patient safety context with a collaborative team.