Spec QA DMR

Medline Industries, LP

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Wuhan 武汉 Until 8/28/2026 H-1B sponsor history First posted June 29, 2026 Last posted June 29, 2026
Job description

Job Summary

QA Specialist is responsible for quality assurance on the procedures of DMR and inspection criteria development and maintenance. Work closely with divisional QA and Asia stakeholders to ensure requirements are met under ISO13458 and CFR820.

Job Description

(1)    Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan;

(2)    Establish inspection criteria of new finished products, update and maintain inspection criteria for existing products on Medline quality management platform (ETQ)

(3)    Maintain functions of inspection criteria in Medline quality management platform (ETQ) available for inspection

(4)    Provide training to internal and external stakeholders on the procedure and requirement of DMR and inspection criteria when necessary.

(5)    Conduct change control by reviewing documents provided by suppliers who have submitted the requests, and assist in helping suppliers complete the changes.

(6)    Conduct sample construction review for new products, and assist in helping suppliers understand the product specification

(7)    Complete monthly Complaint Trending Report and make adjustment as requirement of DQA if some improvement is needed.

(8)    Complete Supplier Re-Evaluation by reviewing suppliers who have already been processed through the Vendor Evaluation Procedure and their approximate three-year review is approaching and providing corresponding dispositions

(9)    Review the Component Sourcing Form completed by suppliers and assign Quality Warnings (QW Codes) based on the suppliers’ review results.

(10) Implement the improvement plan and standardize the processes if necessary and share good experience with team members.

(11) Other projects assigned by managers/DQAs.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

About this role

Summary

Ensure quality of device procedures, inspection standards, and compliance with regulations.

Job title

Spec QA DMR

Experience level

not specified

Industry

healthcare

Location requirements

Wuhan, on-site; remote not indicated.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

document reviewinspection criteriaISO13458CFR820training

Preferred skills

None specified

Specializations

documentation reviewinspection criteriaISO13458CFR820
Locations

Structured locations inferred from the posting.

Wuhan, Hubei, China

On-site City
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