Career Management Group
Senior Supplier Quality Engineer
Career Management Group, Bothell, Washington, United States, 98021
Overview
Position:
Senior Supplier Quality Engineer Location:
Bothell, WA Employment type:
Full-Time | Onsite Contract:
6-month contract with potential extension Base pay range (provided by Career Management Group):
$60.00/hr - $80.00/hr Note:
Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. What You’ll Do
Support manufacturing operations by resolving and preventing supplier-caused non-conformances Lead supplier quality system and process audits (domestic & international) Conduct and document part and process qualification activities Drive process improvements using supplier quality metrics Partner cross-functionally to prevent part shortages and ensure compliance with 21 CFR 820 and ISO 13485:2016 Evaluate and support the selection of new suppliers Qualifications
Required: 5+ years in engineering, supplier quality, or similar (medical device industry preferred) Bachelor’s degree in engineering or life sciences Strong communication, documentation, and organizational skills Knowledge of 21 CFR 820 & ISO 13485:2016 Preferred: Master’s degree in engineering or life sciences Experience auditing domestic & international suppliers Additional notes
This is an excellent opportunity for a quality-focused engineer to make an impact in the medical device industry while working onsite in a collaborative, fast-paced environment.
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Position:
Senior Supplier Quality Engineer Location:
Bothell, WA Employment type:
Full-Time | Onsite Contract:
6-month contract with potential extension Base pay range (provided by Career Management Group):
$60.00/hr - $80.00/hr Note:
Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. What You’ll Do
Support manufacturing operations by resolving and preventing supplier-caused non-conformances Lead supplier quality system and process audits (domestic & international) Conduct and document part and process qualification activities Drive process improvements using supplier quality metrics Partner cross-functionally to prevent part shortages and ensure compliance with 21 CFR 820 and ISO 13485:2016 Evaluate and support the selection of new suppliers Qualifications
Required: 5+ years in engineering, supplier quality, or similar (medical device industry preferred) Bachelor’s degree in engineering or life sciences Strong communication, documentation, and organizational skills Knowledge of 21 CFR 820 & ISO 13485:2016 Preferred: Master’s degree in engineering or life sciences Experience auditing domestic & international suppliers Additional notes
This is an excellent opportunity for a quality-focused engineer to make an impact in the medical device industry while working onsite in a collaborative, fast-paced environment.
#J-18808-Ljbffr