Quality Control Inspector: Medical Devices

Mevion Medical Systems; Littleton (MA); On-site; USD 47,000 - 50,000; Full time

Job summary

Mevion Medical Systems in Littleton, MA is seeking a Contract Quality Control Inspector to ensure incoming, in-process, and finished components meet quality standards. This role requires 3+ years in QC and familiarity with FDA/ISO 13485 guidelines.

You will perform inspections, document records, interpret drawings with GD&T, and support audits. This contractor position may involve lifting up to 20 lbs in a fast-paced manufacturing environment.

Qualifications

• High school diploma or equivalent required.
• Associate degree or higher a plus.
• At least 3 years in Quality Control in medical devices preferred.
• Strong knowledge of GD&T and mechanical drawings required.
• Proficient with inspection tools (calipers, micrometers, etc.).
• Familiar with ERP and document control systems.
• Detail-oriented with able to work independently in a fast-paced environment.
• Excellent communication with internal customers.

Responsibilities

• Perform dimensional, visual, and functional inspections of components, subassemblies, and finished assemblies.
• Conduct first article inspections (FAI), in-process inspections, and final inspections.
• Document and maintain inspection reports and quality records.
• Interpret drawings and GD&T symbols to ensure compliance.
• Maintain inspection equipment calibration and proper use of tools.
• Document and process non-conforming issues.
• Support internal and external audits with inspection records.
• Assist Quality Control and Calibration improvement projects.
• May lift up to 20 lbs with hoist or lifting devices.

Skills

GD&T

Inspection

Quality control

Documentation

Education

High school diploma or equivalent

Associate degree or higher (plus)

Tools

Calipers

Micrometers

Micro-Hite

Plug gauges

Thread gauges

Job description

Mevion Medical Systems in Littleton, MA is seeking a Contract Quality Control Inspector to ensure incoming, in-process, and finished components meet quality standards. This role requires 3+ years in QC and familiarity with FDA/ISO 13485 guidelines.

You will perform inspections, document records, interpret drawings with GD&T, and support audits. This contractor position may involve lifting up to 20 lbs in a fast-paced manufacturing environment.