Medical Device Incoming Materials QA Inspector

Torrey Holistics; Minneapolis (MN); On-site; USD 28,000 - 32,000; Full time

Benefits offered by this job

Bi-weekly pay

Medical insurance

Dental insurance

Vision insurance

401(k) with company match

PTO

Maternity leave

Paternal leave

Tuition reimbursement

Continuing education

Advancement opportunities

Job summary

Torrey Holistics in Plymouth, MN is seeking an Incoming Materials Quality Specialist to inspect incoming components and in-process assemblies, ensuring compliance with ISO 9001/13485 and FDA requirements. You will document measurements, flag nonconformances, and support the Material Review Board with timely dispositions.

You'll work with SAP records, calibration logs, and quality documentation, collaborating with the team to drive accuracy and continuous improvement in a fast-paced environment.

Qualifications

• High school diploma or GED and at least 1 year in mechanical inspection or similar production tasks.
• Comfort with PCs and desktop apps (Excel, Word) and good documentation habits.
• Ability to manage multiple priorities and work in a fast-paced environment.
• Collaborative mindset and professional team-focused approach.

Responsibilities

• Conduct precise inspections of incoming components and in-process assemblies using calipers, micrometers, gauges, and other metrology tools.
• Flag, segregate, and document nonconforming material and participate on the Material Review Board.
• Support NC disposition activities and re-inspection/verification.
• Enter and retrieve inspection data in SAP and maintain quality records (DHRs, calibration logs).
• Collaborate on problem solving and continuous improvement activities.

Skills

Quality inspection

Medical devices

SAP

Calipers

Micrometers

Documentation

Problem solving

Team collaboration

Education

High school diploma or GED

Tools

Calipers

Micrometers

Gauges

SAP

Rulers

Metallurgy tools

Job description

Torrey Holistics in Plymouth, MN is seeking an Incoming Materials Quality Specialist to inspect incoming components and in-process assemblies, ensuring compliance with ISO 9001/13485 and FDA requirements. You will document measurements, flag nonconformances, and support the Material Review Board with timely dispositions.

You'll work with SAP records, calibration logs, and quality documentation, collaborating with the team to drive accuracy and continuous improvement in a fast-paced environment.