We are seeking a highly experienced Quality Assurance Engineer – Design Quality Focus to support New Product Development and Sustaining Product Development initiatives within a highly regulated medical device environment. The ideal candidate will have a strong background in Biomedical or Mechanical Engineering , with hands‑on experience in Design Quality, Quality Assurance, Risk Management, ISO/FDA compliance, and regulated product development .
The Quality Assurance Engineer will serve as a key QA representative on product development initiatives and will be responsible for ensuring compliance with internal quality systems, government regulations, and applicable industry standards.
Key Responsibilities
- Participate in design and manufacturing reviews throughout product development activities.
- Generate and review DFMEAs/UFMEAs and participate in risk analysis and risk management discussions .
- Review and approve design and development documentation .
- Serve as a Design Quality Subject Matter Expert during ISO and FDA audits .
- Author and maintain quality system procedures, work instructions, and technical documentation .
- Conduct internal audits of quality systems and other business functions.
- Evaluate nonconforming materials and support disposition decisions through cross‑functional engineering reviews.
- Ensure compliance with internal and external specifications, GMP, ISO, FDA, and applicable medical device regulations .
- Review trends associated with device failures, customer complaints, and nonconforming materials .
- Lead and own Corrective and Preventive Actions (CAPA) .
- Participate in Health Hazard Evaluations and product safety assessments.
- Support New Product Development (NPD) and Sustaining Product Development initiatives.
- Work closely with Engineering, Manufacturing, Quality, and other cross‑functional teams.
- Support complex quality and engineering projects as assigned.
- Ensure quality processes and documentation meet applicable regulatory and company requirements .
Required Skills
- Bachelor’s degree in Biomedical Engineering or Mechanical Engineering .
- 3+ years of engineering experience , including at least 1 year in a design‑focused environment , or an equivalent combination of education and experience.
- Professional experience within a Medical Device, Aeronautics, Automotive, or other highly regulated industry .
- Strong understanding of Design Quality and Quality Assurance principles .
- Experience with ISO 13485 quality standards preferred.
- Strong knowledge of technical writing, quality documentation, procedures, and work instructions .
- Knowledge of manufacturing processes , including:
- Metrology
- Precision machining
- Grinding
- Product cleaning
- Strong understanding of quality systems, compliance, and regulatory requirements .
- Knowledge of Microsoft Office Suite or equivalent productivity tools.
- Strong analytical, problem‑solving, communication, and documentation skills .
- Detail‑oriented with the ability to manage complex quality activities in a regulated environment.
Preferred Skills
- Advanced knowledge of ISO 14971 and medical device risk management principles .
- Experience with SolidWorks .
- Experience with SolidWorks ePDM .Experience with Oracle R12 .
- Experience with Agile PLM .
- CQE, Lean, or Six Sigma certification .
- Experience supporting FDA and ISO audits .
- Experience with CAPA, nonconformance, complaint trending, and risk analysis .
- Strong understanding of GMP and medical device quality systems .
- Experience working within New Product Development and Sustaining Engineering environments.
ABOUT BRICKRED SYSTEMS
BrickRed Systems is a global leader in next‑generation technology consulting and workforce solutions, specializing in delivering high‑quality talent across digital, engineering, marketing, analytics, finance, operations, and business transformation domains. With a strong emphasis on innovation, scalability, and client success, BrickRed Systems helps organizations solve complex business challenges by providing skilled professionals across strategy, technology, creative, and operational functions. BrickRed fosters a culture of continuous learning, collaboration, and excellence, enabling professionals to contribute to high‑impact global initiatives while advancing their careers.
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This position is listed as full time and onsite.