Job Details

ID #21203979
State California
City San diego
Job type Contract
Salary USD $52 52
Source Stellar Consulting Solutions
Showed 2021-10-16
Date 2021-10-15
Deadline 2021-12-13
Category Et cetera
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Engr 2, Hardware Quality

California, San diego, 92121 San diego USA

Vacancy expired!

Stellar Consulting Solutions is a boutique business & technology consulting company headquartered in Atlanta, GA. We deliver high quality, agile, and experienced workforce for niche technology projects of any scale. We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly to match skill supply and demand on a real-time basis. Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and retain qualified talent. We have a stellar reputation for striving to achieve high ethical standards. Our use of Innovative techniques and industry best practices has made us one of the fastest growing boutique firms delivering to enterprise business. Description: Responsibilities: Supports supplier qualification/approval process by assessing supplier QMS as well as manufacturing and technology capabilities through onsite and virtual audit activities Supports design, development, and manufacturing operations toward resolution of supplier quality problems as well as the implementation of corrections and corrective actions Works with suppliers to establish and maintain robust/rigorous measurement methodologies Partners with suppliers to establish and maintain controlled manufacturing processes Facilitates root cause analysis and corrective actions for supplier quality issues (SCARs) Drives supplier validation activities using Advanced Product Quality Planning (APQP) Drives supplier Production Part Approval Process (PPAP) activities Reports supplier quality trends, performance, and other information to leadership Travel up to 25% may be required Qualification: Bachelor's degree in an engineering discipline is required A minimum of 3 year's experience in a Supplier Quality engineering role is required Prior experience within a regulated industry (e.g. medical device, pharma) is required ISO 13485 Lead Auditor certification is required Demonstrated knowledge of the Quality Engineering body of knowledge is required Demonstrable good communication and strong writing skills are required Familiarity with PCB, PCBA, and electro-mechanical assemblies is a plus. ASQ certifications are a plus Working knowledge of DMAIC\Six Sigma and problem-solving methodologies is a plus. Candidate must be able to work autonomously and independently

Vacancy expired!

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