Incoming Materials Quality Specialist (Medical Devices)

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

Incoming Materials Quality Specialist (Medical Devices)Join our Plymouth, MN team and be a frontline guardian of product quality in a highly regulated environment. In this role, you help operate and improve the site’s quality system aligned with ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, and EU MDR. Your expertise ensures components and in-process products meet exacting standards before they move forward.At-a-GlanceHours: Monday–Friday day shift (start at 6/7/8am) with overtime as neededPay: $20–$23 per hour + quarterly bonus & meritLocation: 14605 28th Ave North, Plymouth, MNHire Type: Direct, full-timeA Day in the LifeConduct precise inspections of incoming components and in-process assemblies using calipers, micrometers, gauges, and other standard metrology tools.Flag, segregate, and document nonconforming material; maintain clear, complete records.Participate on the Material Review Board, contributing to decisions on nonconformance reports and appropriate dispositions.Support nonconformance (NC) disposition activities, including re-inspection and verification.Enter and retrieve inspection and NC data within local and global systems (e.g., SAP), producing accurate, high-quality documentation.Review associated quality records such as Device History Records (DHRs) and equipment calibration logs.Partner with the team on problem-solving and continuous improvement opportunities; perform additional duties as assigned.Tools & Systems You’ll UseMeasurement gauges, calipers, and micrometersSAP for documentation and data retrievalMicrosoft Excel and Word for reporting and recordsRequired QualificationsHigh school diploma/GED and at least 1 year in mechanical inspection or other technical production tasks.Comfort with PCs and common desktop apps (Excel, Word).Ability to thrive in a fast-paced, deadline-driven setting while producing meticulous documentation.Collaborative approach to analyzing and resolving technical issues; capable of managing multiple priorities in parallel.Professional, team-first mindset.Preferred QualificationsExperience in Continuous Improvement (CI) or 5S practices.More than 1 year as a Quality Inspector within medical device manufacturing/production.Hands-on experience with component inspection in a medical device setting.Prior experience recording information in SAP or a similar system.Working knowledge of calipers, rulers, and metallurgy tools.Exceptional attention to detail and adherence to procedures.Physical RequirementsLift/push/pull 25–50 lbs.Frequent bending, walking, standing, sitting, and typing.Manual dexterity/hand manipulation and strong visual acuity.Benefits & GrowthWe’re committed to supporting your health, well-being, and long-term success.Market-competitive, bi-weekly payBenefits effective after 30 daysGenerous PTO plus additional holidaysComprehensive medical, dental, and vision coverageShort- and long-term disability401(k) with company matchMaternity and paternal leaveOptional add-ons/discounts (e.g., Pet Insurance)Tuition reimbursement and continuing education supportClear paths for advancement and a stable, long-term careerProficiency SpotlightQuality inspection and component inspectionWeighing raw materialsComposite materials and repairISO 9001 familiarityMedical device environment exposureMicrosoft Excel and WordSAPTechnologies You’ll TouchMeasurement gaugesCalipers and micrometersSAP