Quality Inspector (Weekend Shift) We are seeking a detail-oriented Quality Inspector to perform incoming and in-process inspection of machined, stamped, molded, formed, and assembled components used in medical devices, with a focus on surgical retraction instruments, sterilization cases/trays, and related medical device accessories. Additionally, the role will support audits and quality system activities; investigate nonconformances; and ensure compliance with customer, regulatory, and company requirements. The ideal candidate has a sharp eye for detail, strong knowledge of inspection tools and techniques, and experience working in a regulated medical device manufacturing environment. The schedule for this role is

Friday, Saturday, Sunday:

5:00 AM - 5:00 PM. Thompson is employee-owned and vested employees automatically receive company shares.

What You'll Do:

Verify product quantities and documentation, identify nonconformances, and coordinate rework, rejection, or corrective actions with Production as needed. Review operator, supplier, and production documentation for completeness and compliance prior to inspection or product release. Perform inspection of incoming raw materials and purchased components, in-process, and finished products for dimensional accuracy, surface finish, functionality, and cosmetic quality ensuring compliance with specifications, customer requirements, and company standards. Inspect and verify parts returned from outsourced special processes, including electropolish, coatings (e.g., anodizing, PVD, passivation), and heat treatment, ensuring compliance with process certifications and specs. Use precision measuring instruments (calipers, micrometers, height gauges, optical comparators, CMM, thread gauges, etc.) to verify dimensional conformance. Review and verify certificates of conformance, material certs, and process certifications from suppliers and outside processors. Print, apply, and verify product labels and barcodes as required. Verify, review, complete work orders and associated documentation within the ERP system. Support first article inspections (FAIs), Controlled and Engineering builds, finished goods sampling, and routine product audits. Record, review, and maintain receiving and in process inspection logs, inspection records, scanned documents, and other quality system documentation in accordance with company procedures. Maintain compliance with

ISO 13485, FDA 21 CFR

Part 820, and internal quality system procedures and recommend updates when improvements or changes are needed. Respond to internal quality support requests and assist with quality-related issues throughout the organization. Monitor production processes and equipment to ensure conformance to established requirements and support continuous improvement initiatives.

This Might Describe You :

High school diploma or equivalent required; technical/vocational training in quality inspection, machining, or manufacturing a plus. 2+ years of quality inspection experience in a manufacturing environment; medical device experience preferred. Ability to read and interpret engineering drawings, GD&T, and specifications. Hands-on experience with precision measuring instruments and inspection equipment. Working knowledge of ISO 13485 and/or FDA QSR (21 CFR Part 820) preferred. Strong attention to detail and documentation accuracy. Basic computer skills (ERP/QMS data entry, Microsoft Office). Ability to work independently during weekend shift hours with minimal on-site supervision.

Physical Requirements:

Ability to stand/sit for extended periods during 12-hour shifts. Ability to lift 25-35 lbs. occasionally. Manual dexterity for handling small precision parts and inspection tools. Visual acuity for detailed inspection work (corrected vision acceptable).

EEO/AA Benefits:

401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Parental leave Retirement plan Vision insurance

Work Location:

In person