Caris Life Sciences · 1 day ago
Supplier Quality Engineer
Phoenix, AZ
Full-time
Onsite
Mid Level
3+ years expCaris Life Sciences is a pioneering company in precision medicine and is dedicated to transforming cancer care. The Supplier Quality Engineer is responsible for ensuring quality from suppliers and providing technical support, while also acting as a liaison to drive continuous improvement and address quality issues.
Artificial Intelligence (AI)BiopharmaBiotechnologyHealth CareLife Science
Responsibilities
Responsible for the appropriate qualification and on-going monitoring of Caris’ suppliers
Assist in performing supplier audits providing subject matter expertise. Can lead supplier audits based on auditor qualifications
Assess and critique supplier process control documentation, identifying areas of improvement and driving improvement within the suppliers’ QMS
Open and assist with Supplier Corrective Action Request, ensuring effective use of appropriate problem-solving tools
Performs critical assessment of internal and supplier proposed change management activities
Provide education and training to suppliers as necessary
Provide problem solving expertise at site and supplier locations in support of critical quality issues
Assist with development of effective quality improvement plans to be implemented at appropriate suppliers
Collaborate with internal teams to gather assessments for supplier-initiated changes requests for continuous improvement, cost reduction or supplier remediation activities
Support tracking and reporting of KPI and other metrics associated with supplier performance
Articulate detailed supplier performance results and trends to appropriate levels of management
Perform detailed process reviews at supplier's manufacturing site
Maintain and track to completion closure of assigned supplier action items
Develop relationships with suppliers and internal cross functional partners
Analyze non-conformance data to prioritize projects and to solve systemic supplier issues
Assist, as needed, to perform other related duties and special projects as required
Qualification
Required
Bachelor's degree in engineering required
Strong knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics)
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use
Preferred
A minimum of 3 years of experience working within FDA regulated (Medical Device) or regulated industries (Automotive, Aerospace) highly preferred
Quality Auditor Qualification preferred (ISO 13485, CFR 820 or comparable industry standard and regulatory requirements)
Company
Caris Life Sciences
Caris Life Sciences develops molecular profiling and AI-driven technologies to support precision medicine in oncology.
1001-5000 employees
Funding
Current Stage
Public CompanyTotal Funding
$1.86BKey Investors
BraidwellOrbiMedSixth Street
2025-06-18IPO
2025-04-07Private Equity· $168M
2023-01-19Debt Financing· $400M
Leadership Team
Luke Power
Chief Financial Officer
Brian Stengle
SVP, Chief Marketing Officer
Recent News
2025-12-22
2025-12-21
2025-12-19
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