Quality Inspector - Medical Device Manufacturing

Hu-Friedy Mfg. Co., LLC; Phoenix (AZ); On-site; USD 25,000 - 32,000; Full time

Benefits offered by this job

Quarterly Bonuses

401K Match

PTO

Company Holidays

Healthcare benefits

Tuition assistance

Job summary

HuFriedyGroup is seeking a Quality Inspector in Phoenix, AZ to assist in ISO 9001/13485 and related regulatory compliance. You will perform incoming, in-process, and final inspections using standard measurement equipment and document NCs for MRB review.

Ideal candidates have 1–2 years in manufacturing or quality, can read blueprints, and generate precise documentation. The role includes healthcare benefits, PTO, and opportunities for growth in a collaborative team environment.

Qualifications

• 1–2 years' experience in manufacturing or quality.
• Ability to read and interpret blueprints.
• Ability to generate detailed, high-quality documentation.
• Ability to collaborate to analyze and solve technical problems.
• Attention to detail and interpreting written instructions.
• Good written and verbal communication.

Responsibilities

• Conduct component and assembly incoming, in-process, and final product inspections to appropriate standards utilizing blueprints and inspection measurement equipment.
• Identifies, segregates and documents rejected components and materials.
• Participates on a Material Review Board to review and process non conformance reports.
• Enters and retrieves inspection and NC data from local and global systems.
• Reviews related Quality documentation such as DHR’s or calibration records.
• Supports local problem solving activities and may identify opportunities for improvement.
• Complete other duties as assigned.

Skills

Blueprint reading

Attention to detail

Problem solving

Communication skills

Job description

HuFriedyGroup is seeking a Quality Inspector in Phoenix, AZ to assist in ISO 9001/13485 and related regulatory compliance. You will perform incoming, in-process, and final inspections using standard measurement equipment and document NCs for MRB review.

Ideal candidates have 1–2 years in manufacturing or quality, can read blueprints, and generate precise documentation. The role includes healthcare benefits, PTO, and opportunities for growth in a collaborative team environment.