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Design Quality Engineer

Design Quality Engineer

BioTalentSan Diego, CA, United States
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Quality Engineer / Senior Quality Engineer

Location : San Diego, CA (Hybrid)

We’re seeking a hands-on and detail-oriented Quality Engineer to join our growing Quality Assurance and Regulatory Affairs team. The ideal candidate will have a strong engineering background with experience across the full product lifecycle—from design through manufacturing—within the medical device industry.

This individual will play a key role in shaping and strengthening our Quality Management System (QMS), with opportunities to lead validation, process improvement, and regulatory readiness initiatives.

Role & Responsibilities

  • Partner with R&D to define product requirements and release criteria; support design reviews and ensure robust technical documentation.
  • Lead risk management activities (FMEA / DFMEA / PFMEA) and maintain traceability throughout the design process.
  • Author, maintain, and execute design verification and validation (V&V) protocols and reports; lead hands-on test method validations (TMVs) and formal V&V testing.
  • Execute and document intended-use and computer system validations , ensuring systems meet regulatory and business needs.
  • Drive QMS remediation and continuous improvement initiatives —identify procedural or documentation gaps proactively, develop and implement sustainable fixes, and ensure alignment with FDA QMSR and ISO 13485.
  • Draft, revise, and maintain SOPs and quality procedures ; support internal audits, CAPA, and monitoring of quality metrics.
  • Contribute to regulatory submissions (e.g., 510(k), Letters to File, labeling, technical documentation) and ensure compliance with global regulatory standards.
  • Oversee supplier qualification , conduct supplier audits, and drive supplier corrective and preventive actions (SCARs).
  • Develop inspection plans; support inventory control, equipment / tool calibration, and process validation (IQ / OQ / PQ) activities.
  • Collaborate across Operations, Manufacturing, and Supply Chain to communicate risks, mitigations, and timelines effectively.
  • Mentor junior team members and help foster a culture of continuous learning and improvement.

Requirements

  • Bachelor’s degree in Engineering or a related technical field.
  • 2–4 years of quality engineering experience in the medical device or diagnostics industry (additional experience considered for Senior title).
  • Working knowledge of FDA QMSR, ISO 13485, ISO 14971 , and experience with lifecycle documentation in regulated environments.
  • Proven experience in QMS remediation or enhancement —demonstrated ability to identify process or documentation gaps and implement proactive, scalable solutions.
  • Hands-on validation experience (e.g., developing and executing TMV, IQ / OQ / PQ, and process validation activities).
  • Preferred familiarity with 510(k) submissions and / or EU MDR technical documentation.
  • Exposure to early-stage or startup environments where adaptability and cross-functional collaboration are key.
  • Strong technical writing, attention to detail, and data-driven problem-solving skills.
  • Excellent communication and stakeholder management skills; able to clearly articulate findings, risk assessments, and recommendations.
  • Ambitious, career-driven, and self-motivated —someone with a clear vision for their professional growth and the drive to make an impact in a scaling organization.
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