Engineer QA

Posted 2 Days Ago
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Shanghai, Shanghai Municipality, Shanghai, CHN
In-Office
Entry level
Other
No.1 privately held manufacturer & distributor of health care products in the U.S.
The Role
Ensures suppliers meet company and international medical device quality standards. Performs product verification, process audits, testing, root-cause investigations, CAPA implementation, supplier quality improvement, complaint resolution, production parameter validation, and rejection reduction. Collaborates with quality, project management, corporate, and China-based QC teams to improve product and process performance, maintain compliance, and achieve cost savings.
Summary Generated by Built In

Job Summary

Job Description

1. Ensure suppliers are clear on all Company and International standards, processes and procedures as they relate to various medical devices.

2. Perform in line and finished product verification in accordance with Company and International Standard to ensure acceptable quality.

3. Work with other functional team (QA and PM) to determine appropriate testing parameters for the products to ensure limited failures in product.

4. Perform process audits and identify opportunities for continuous improvement on process control, production control and quality control.

5. Be responsible for projects with vendors from a quality perspective, more specifically, on product design change, quality performance improvement, and monitoring quality performance on critical products.

6. Work with Suppliers and Company corporate office in US to help resolve various customer complaints. Specifically, help with root cause investigations and analysis. Implement CAPAs based on root cause investigations to reduce complaint numbers. Ensure that solutions to quality issues are properly implemented and upheld.

7. Work with suppliers and Company QC team in China to reduce product rejections.

8. Work with suppliers to identify opportunities for product and process improvements that lead to cost savings.

9. Work with supplier to validate and optimize the production parameters and ensure suppliers properly document and verify these parameters once implemented.

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.

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The Company
HQ: Northfield, IL
20,000 Employees
Year Founded: 1961

What We Do

All across America and the world, we help healthcare systems improve patient outcomes and reduce costs through clinical and financial solutions. As both a manufacturer and distributor of medical devices and supplies, we’re made up of problem solvers. Risk-takers. Big thinkers and doers.

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