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Senior Quality Engineer - CONTRACT POSITION
Senior Quality Engineer - CONTRACT POSITIONBioTalent • Carlsbad, CA, US
Senior Quality Engineer - CONTRACT POSITION

Senior Quality Engineer - CONTRACT POSITION

BioTalent • Carlsbad, CA, US
Hace 1 día
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

Job Description

  • 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 You’ll 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 You’ll Bring

  • Bachelor’s 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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    Senior Quality Engineer • Carlsbad, CA, US

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