Quality Engineer / Senior Quality Engineer
Location : San Diego, CA (Hybrid)
Were 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 lifecyclefrom design through manufacturingwithin 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
Bachelors degree in Engineering or a related technical field.24 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.