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Spec QA DMR

Wuhan 武汉💼 Full-time🗓 2026-08-13 → 2026-09-26

Core

Collect and review Device Master Record (DMR) documents, establish and maintain inspection criteria, and conduct supplier quality reviews for Medline products.

Role type

Spec QA DMR Specialist

Builds

Medline medical products

Domain

Medical Devices / Quality Assurance

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

DMR document review, inspection criteria management, supplier evaluation, change control, complaint trending analysis, quality warning assignment

Preferred skills

process improvement, training delivery, cross-functional collaboration

Technologies

ETQ

Responsibilities

Collect and review DMR documents for regulatory compliance; Establish and maintain inspection criteria on the quality management platform; Conduct change control for supplier submissions; Complete monthly Complaint Trending Reports; Perform Supplier Re-Evaluations; Review Component Sourcing Forms and assign Quality Warnings.

Seniority

Individual Contributor

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