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Quality Engineer (Carlsbad)
Quality Engineer (Carlsbad)BioTalent • Carlsbad, CA, US
Quality Engineer (Carlsbad)

Quality Engineer (Carlsbad)

BioTalent • Carlsbad, CA, US
Hace 4 días
Tipo de contrato
  • A tiempo parcial
Descripción del trabajo
  • NO C2C OR THIRD PARTIES
  • Duration : 6-months with potential for extension
  • Location : on-site 4x per week in Carlsbad, CA
  • Hourly rate : $40-55 / hr DOE
  • Join an innovative medical-device team focused on improving patient outcomes through engineering excellence and regulatory precision. The Quality Engineer / Senior Quality Engineer will play a key role in ensuring compliance, reliability, and performance of life-changing technologies supporting both product development and ongoing manufacturing operations.

    What Youll Do

    • Develop and maintain quality controls, processes, and analytical methods to ensure conformance to product specifications.
    • Lead verification and validation (V&V) testing, including protocol design, execution, data analysis, and reporting.
    • Support design control activities and cross-functional reviews for new product development and significant design changes.
    • Drive statistical analysis and data-driven decision making for process stability and product quality.
    • Collaborate with manufacturing and suppliers to maintain conformance and improve assembly, testing, and documentation practices.
    • Support supplier qualification , incoming inspection, and process improvement initiatives.
    • Participate in risk management activities (ISO 14971) and ensure compliance with QMS and regulatory standards.
    • Support internal and external audits (FDA, ISO), nonconformance investigations, and CAPA initiatives.
    • Analyze field issues and deviations, perform root cause analysis, and implement effective corrective actions.
    • What Youll Bring

    • Bachelors degree in Biomedical, Mechanical, Chemical, or related Engineering field .
    • 3-5+ years of experience in a medical device quality engineering role.
    • Working knowledge of FDA QSR, ISO 13485, ISO 14971 , and risk-based quality systems.
    • Hands-on experience with verification testing, statistical analysis, and process validation .
    • Strong communication skills able to produce clear reports, present findings, and collaborate across disciplines.
    • Proficiency with Excel, Minitab, MATLAB , or equivalent analytical tools.
    • Detail-oriented, organized, and proactive in driving continuous improvement.
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    Quality Engineer • Carlsbad, CA, US

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