Quality Engineer

Quality Engineer II

Works closely with development/manufacturing/quality engineering to establish and ensure compliance and quality for product related risk management documentation. Ensure risk management assessments and evaluations for products conform to established standards and agency regulations. This role will support product risk management activities across the product lifecycle, including evaluating risks associated with complaints, manufacturing non-conformances, and new product development. The Quality Engineer II will work cross-functionally with Engineering, Manufacturing, Regulatory, and Quality teams to establish and maintain compliant risk management documentation in alignment with FDA regulations and ISO standards.

Responsibilities include performing hazard and risk assessments, contributing to continuous improvement of risk management processes, and ensuring product risk documentation is accurate, complete, and audit-ready. A strong understanding of complaint handling, health hazard assessments, and medical device regulatory environments is preferred.

Bachelor's degree in Engineering or related technical field. Minimum 3 years of experience in quality engineering within a regulated environment (medical device, pharmaceutical, or similar). Hands-on experience with product risk management, including hazard analysis and risk assessments (ISO 14971). Experience supporting complaint investigations, non-conformance evaluations, or health hazard assessments. Working knowledge of FDA regulations, ISO standards, and quality systems. Proven ability to collaborate cross-functionally with Engineering, Manufacturing, and Regulatory teams.

Strong analytical, problem-solving, and documentation skills.

Certified Quality Engineer (CQE) or equivalent. Experience with GMP environments and quality system audits. Exposure to new product development and design assurance activities.