- Bridgeport, CT (from $ 82,524 to $ 168,219 year)
- Santa Ana, CA (from $ 74,278 to $ 159,732 year)
- Santa Rosa, CA (from $ 75,166 to $ 159,508 year)
- Santa Clara, CA (from $ 75,860 to $ 159,471 year)
- Fremont, CA (from $ 63,375 to $ 159,400 year)
- San Bernardino, CA (from $ 59,423 to $ 154,536 year)
- Seattle, WA (from $ 62,500 to $ 154,010 year)
- San Mateo, CA (from $ 59,421 to $ 153,946 year)
- San Jose, CA (from $ 59,668 to $ 152,424 year)
- San Diego, CA (from $ 60,109 to $ 152,330 year)
Qa Jobs in USA
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Qa • usa
Sr QA Specialist - Supplier QA
Insight GlobalSouth San Francisco, CA, United States- Promoted
Automation QA
Compunnel, Inc.Littleton, CO, US- Promoted
Senior QA Automation Engineer
QAOrlando, FL, US- Promoted
QA Technician
QualiTechChaska, MN, United States- Promoted
QA Engineer
SupplyHouseAtlanta, GA, United StatesQA Analyst -
Simarn SolutionsCalifornia, Michigan, United StatesQA
Diverse LynxColumbus, OH, United States- Promoted
- New!
QA Engineer
KuvareDes Moines, IA, US- Promoted
QA Technician
Tandem FoodsPittsburgh, PA, US- Promoted
QA ENGINEER
AaraTechnologies IncFort Worth, TX, US- Promoted
QA Inspector
MIlls Marine Ship RepairNewport News, VA, USQA Engineer
Nextdata Technologies IncSan Francisco, California, United StatesQA Tester
Stratosphere Games GmbhRemote, Remote, United States- Promoted
QA Engineer
HiltermannleaseHolland, MI, US- Promoted
QA Tech
Diversified Sourcing SolutionsWaxahachie, TX, US- Promoted
QA Engineer
Sonepar USABroomfield, CO, United States- Promoted
QA Engineer
DardenOrlando, FL, USQA Engineer
Nlign Analytics, IncArlington, Texas, United States- Promoted
- New!
NDE QA Technician / QA Inspector
Wagstaff IncSpokane Valley, WA, United States- Promoted
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Hengrui PharmaPrinceton, NJ, USThe average salary range is between $ 42,898 and $ 117,763 year , with the average salary hovering around $ 77,798 year .
Related searches
Sr QA Specialist - Supplier QA
Insight GlobalSouth San Francisco, CA, United States- Full-time
We are seeking a Senior QA Specialist in Supplier Quality Assurance who will play a critical role in managing and improving supplier and contract manufacturer (CMO) relationships. This person will lead efforts to qualify, monitor, and reassess suppliers-especially during design transfers and new product introductions. This includes conducting audits, managing non-conformances, and ensuring compliance with FDA, ISO 13485, and EU IVDR standards. You'll collaborate closely with R&D, Supply Chain, and external partners to define supplier selection criteria, establish quality agreements, and oversee technical transfers. This is a full-time hybrid role with an anticipated onsite presence of three days per week and approximately 30% travel, primarily domestic with occasional international visits.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity / affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and / or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy : https : / / insightglobal.com / workforce-privacy-policy / .
Required Skills & Experience
- Bachelor's degree in Life Sciences, Engineering, Biomedical Engineering, Biotechnology, or related field
- 5+ years of QA experience in the medical device or IVD industry
- Strong expertise in supplier quality management and CMO oversight
- Deep knowledge of ISO 13485 : 2016, ISO 14971 : 2019, and IVDR (EU 2017 / 746) standards
- Proven experience conducting supplier audits and managing corrective actions
- Experience with design transfer and technical validations
- Ability to manage supplier qualification, monitoring, and reassessment processes
- Excellent communication and documentation skills
- Strong organizational skills and ability to manage multiple projects
- Willingness to travel (~30%) to supplier and CMO sites
Nice to Have Skills & Experience
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and / or other paid time off as provided by applicable law.