Quality Inspector II – Medical Devices (Onsite)

Thornton Tomasetti; Minnetonka (MN); On-site; USD 29,000 - 58,000; Full time

Job summary

Abbott's Minnetonka, MN location in the Vascular Division seeks a Quality Technician II to support quality engineering methods and provide technical quality support across development and manufacturing. This position is onsite and daily presence is required.

You will perform first article inspections, manage final product inspections, calibrate equipment, run Gage R&R studies, and help create control plans while ensuring compliance with FDA, ISO 13485 and QMS requirements in a fast-paced,

Qualifications

• Associates degree or 2-year technical program and demonstrated competence.
• 2–4 years' experience in quality inspection or similar.
• Knowledge of FDA regulations, ISO 13485, and worldwide regulatory requirements.
• Experience with optical measurement equipment, hand tools, gages, and fixture design.
• Good communication, data analysis, and report-writing skills.

Responsibilities

• Perform first article and in-process inspections; document results.
• Support calibration and maintenance of test equipment.
• Create control plans and assist in verifications/validations.
• Ensure compliance with QMS, EMS, and FDA regulations.

Skills

Quality systems knowledge

FDA regulations

ISO 13485

Data analysis

Report writing

Blueprint reading

Sampling techniques

Communication skills

Team collaboration

Education

Associates degree or 2-year technical program

Tools

Optical measurement equipment

Hand tools

Gages

Fixture design

Calibration tools

Job description

Abbott's Minnetonka, MN location in the Vascular Division seeks a Quality Technician II to support quality engineering methods and provide technical quality support across development and manufacturing. This position is onsite and daily presence is required.

You will perform first article inspections, manage final product inspections, calibrate equipment, run Gage R&R studies, and help create control plans while ensuring compliance with FDA, ISO 13485 and QMS requirements in a fast-paced,