Medical Device Production Inspector – Quality & Compliance

Technical Needs; Manchester (NH); On-site; USD 52,000 - 76,000; Full time

Job summary

Technical Needs is seeking a Production Quality Inspector for an innovative medical device manufacturing facility in Manchester, NH. The role focuses on inspection, testing, and documentation of mechanical and electrical assemblies to ensure product quality and safety.

The ideal candidate has at least 3 years of manufacturing experience, strong organizational skills, and effective communication across teams. Knowledge of ISO/QSR and FDA guidelines is preferred.

Qualifications

• Minimum 3 years hands-on manufacturing experience.
• Experience with assembly, testing, and documentation of mechanical and electrical devices.
• Excellent interpersonal and written communication across diverse teams.
• Proficiency with Microsoft Office and basic computer skills.
• Knowledge of ISO, QSR, and FDA guidelines preferred.

Responsibilities

• Evaluate inspecting equipment for safety and functionality.
• Ensure manufactured products meet industry quality standards.
• Inspect finished products for quality and compliance before release.
• Keep detailed records of inspection performance and traceability.
• Support safety programs and maintain a clean, safe work area.
• Engage in continuous improvement activities with cross-functional teams.
• Monitor line efficiency and communicate any production concerns.

Skills

Attention to detail

Communication

Documentation

Manual dexterity

Education

High School Diploma or GED

Tools

Microsoft Office

Job description

Technical Needs is seeking a Production Quality Inspector for an innovative medical device manufacturing facility in Manchester, NH. The role focuses on inspection, testing, and documentation of mechanical and electrical assemblies to ensure product quality and safety.

The ideal candidate has at least 3 years of manufacturing experience, strong organizational skills, and effective communication across teams. Knowledge of ISO/QSR and FDA guidelines is preferred.