Spec 3, Quality Assurance
Job
Mindlance
Irvine, CA (In Person)
$84,354 Salary, Full-Time
Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
75
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Spec 3, Quality Assurance#26-11903
$39.29-$41.82 per hour
Irvine, CA
All On-site Job Description Bill Rate •On site 5 days
Education Bachelor Engineering or Quality Job Summary The Supplier Quality Analyst is responsible for ensuring that suppliers of materials, components, and services used in medical devices consistently meet quality, regulatory, and risk requirements. This role supports compliance with FDA Quality System Regulation (21 CFR 820), ISO 13485 through supplier performance monitoring, corrective action management, and risk-based supplier controls. Key Responsibilities Manage and maintain supplier qualification, monitoring, and re-evaluation activities in accordance with 21 CFR 820.50 (Purchasing Controls) and
ISO 13485.
Monitor supplier quality performance using KPIs such as defect rates, corrective action trends, and supplier risk levels. Maintain approved supplier lists (ASL) and supplier quality records per document control requirements. Issue, track, and evaluate Supplier change requests. Escalate supplier quality risks and support remediation and improvement plans. Review and support supplier-initiated or internally driven changes that may impact product quality or compliance (materials, processes, manufacturing location). Collaborate with Engineering and Regulatory Affairs to assess supplier changes requiring validation, verification, or regulatory impact evaluation. Provide supplier quality input for management reviews and quality metrics. Ensure supplier quality documentation is accurate, complete, and maintained in the electronic Quality Management System (eQMS). Ensure supplier activities comply with internal procedures, regulatory requirements, and quality system expectations. Required Qualifications Bachelor's degree in Engineering, Quality, or a related field; or equivalent experience. 2-5 years of experience in Supplier Quality, Quality Assurance, or Manufacturing within a medical device or other regulated environment. Working knowledge of 21 CFR 820, ISO 13485, and supplier control requirements. Proficiency in Microsoft Excel and data analysis. Key Skills & Competencies Strong understanding of regulated quality systems Analytical, detail-oriented problem-solving mindset Clear written and verbal communication Ability to influence suppliers and internal stakeholders Strong organizational and time-management skillsShift:
[]Start:
[]EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."Similar remote jobs
Volkswagen Group DE
Ashburn, VA
Posted2 days ago
Updated22 hours ago
Similar jobs in Irvine, CA
Amazon
Irvine, CA
Posted2 days ago
Updated22 hours ago
Similar jobs in California
W3global
Los Angeles, CA
Posted2 days ago
Updated22 hours ago