Supplier Quality Engineer

Posted Yesterday
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Hiring Remotely in Bangkok, Phra Nakhon, Bangkok, THA
Remote
Mid level
Other
No.1 privately held manufacturer & distributor of health care products in the U.S.
The Role
Manage assigned suppliers as primary QA contact, perform QMS vigilance audits, drive process validation and CAPA/SCAR resolution, coordinate change requests, transfer QA/QC knowledge to production, track supplier capacity and ratings, and implement supplier quality improvements.
Summary Generated by Built In

Job Summary

Job Description

RESPONSIBILITIES

  • Manages a bucket of suppliers and works as main point of contact window between suppliers and Corporate QA and Shanghai Office QA.
  • Monitors the suppliers’ maintenance of QMS through vigilance audit with primary focus on P&PC and quality control.
  • Supports/Drives the suppliers to build their own master process validation plan and monitor the execution progress;
  • Coordinates and manages non-conformities with all related stakeholders and suppliers.
  • Directs and collaborates with supplier representatives on quality issues (contain but not limit to complaints, rejections, findings…), ensures timely corrective action implementation (CAPA and SCAR) and contributes to supplier quality improvement programs.
  • Works with suppliers on CAPA follow ups as results of QSR and SA (social accountability) audits.
  • Keeps track of suppliers overall capacity and our volume purchased from them.
  • Works with broader Quality Organization to establish and maintain supplier ratings and executes the program to improve ratings of suppliers assigned to him/her when needed.
  • Coordinates the suppliers’ change requests from the initiation to the end, including standardizing the initiation, leading or assisting to review supplier change requests for assessing impact on product quality and QMS, progress communication, etc.;
  • Transition of QA/QC related knowledge from QE to SQE once the supplier is fully approved for mass production. It includes ensuring the related documents transferring from development to mass production, holding pre-production meeting to align inspection attributes with Medline consistently, and training the QCs (both Medline’s and suppliers’) and production personnel, etc.
  • Identifies and implements improvement opportunities to increase the efficiency and effectiveness of the supplier quality engineering and supplier quality management programs.
  • Work with QC/QA to optimize product inspection criteria with LEAN and effective quality inspection purpose.
  • Completes the other tasks assigned by his/her supervisor or the supplier quality manager.

Qualification

Education level: Bachelor degree in engineering field;

3+ years’ experience on supplier quality management with sound improvement knowledge, working in medical device industry is a plus;

Good communication skills, both English and Mandarin;

Team Spirit, Integrity, self-motivated and ready to work under pressure;

Proven learning and adaption capability.

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.

Skills Required

  • Bachelor degree in engineering field
  • 3+ years' experience in supplier quality management
  • Experience with QMS, audits, CAPA, SCAR, and supplier non-conformity management
  • Good communication skills in English and Mandarin
  • Ability to train and transition QA/QC knowledge to production and supplier personnel
  • Team spirit, integrity, self-motivated, and able to work under pressure
  • Working in medical device industry
  • Proven learning and adaptation capability
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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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