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Supplier Quality Specialist III; Contractor

Job in Brisbane, San Mateo County, California, 94005, USA
Listing for: Freenome
Contract position
Listed on 2026-05-09
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, QA Specialist / Manager, Quality Engineering, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Supplier Quality Specialist III (Contractor)
Location: Brisbane

Supplier Quality Specialist III (Contractor)

Brisbane, California

About this opportunity

The Supplier Quality Specialist III/IV plays an integral role in supporting quality activities related to Supplier Management in accordance with FDA, ISO, and other IVD regulations. This individual also supports the company’s quality system activities that comply with the FDA’s Quality System Regulation 21 CFR § 820 and ISO 13485 as well as CLIA, CAP, and applicable state requirements. In this role you will facilitate the supplier compliance program (external audits, drive improvement in supplier performance, supplier development, supplier selection and qualification).

In addition, this role will support the quality assurance activities in partner development as needed.

What you’ll do
  • Maintain the approved supplier list and supplier audit schedule
  • Drive compliance with applicable quality management system requirements, engaging in supplier corrective actions as needed
  • Conduct external and internal quality audits to identify potential areas of risk and drive continuous improvement
  • Lead the establishment of quality agreements with critical suppliers, and ensure quality of supplier records
  • Actively participate in supplier quality related communication and feedback
  • Lead the processing of supplier change notifications
  • Engage directly with Freenome suppliers to drive quality and process improvements in order to continuously improve the quality of product and services received
  • Maintain supplier non‑conformances through closure and effectiveness review, working with impacted departments
  • Maintain organized records that demonstrate compliance with all company processes, regulations, and the company’s QMS
  • Support routine quality processes such as document control, employee training, investigating non‑conformances, quality metrics, etc.
Must haves
  • Minimum of a Bachelor's degree in a life science field (genetics or molecular biology preferred) or equivalent experience
  • 5+ years of experience in manufacturing operations, clinical laboratory operations, quality, or supplier quality
  • ISO 13485 certified Lead Auditor or Certified Quality Auditor (CQA)
  • Effective problem‑solving skills and ability to identify, analyze and solve problems with minimal direction and to escalate concerns to management
  • Proficiency in Word, Excel, PowerPoint or Google Workspace and experience with document management systems and document sharing systems
  • Ability to prioritize and multitask while maintaining a positive and collaborative attitude
  • Experience with both internal and external audits
  • Effective verbal and written communication skills and ability to share and receive information from all levels of the organization across various departments
  • Excellent teamwork skills and the ability to interface effectively with a wide range of stakeholders
  • Flexibility to successfully balance and prioritize multiple ongoing projects/tasks in a fast‑paced, deadline‑driven environment
  • Drive for results and continual improvement
  • Travel 10–30% domestically and potentially internationally, and possibly more as needed
Nice to haves
  • Certified Quality Engineer, CQE (ASQ)
  • Experience in quality system methodologies including but not limited to CAPA, Lean, 5 Why’s, Pareto Analysis, Six Sigma
  • Experience with statistical process control (SPC) techniques to evaluate and improve process performance
  • Experience with process validations
Additional information

Contractors may be hired through a third‑party provider and will be considered contingent workers. We invite you to check out our career page at  for additional company information.

Freenome is proud to be an equal‑opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Applicants have rights under Federal Employment Laws.

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