Design Quality Engineer

Design Quality Engineer Are you passionate about quality, innovation, and patient safety? Do you enjoy working across functions to ensure medical devices remain safe, effective, and compliant throughout their lifecycle? Join Smith+Nephew as a Design Quality Engineer and play a key role in supporting our Sports Medicine Joint Repair portfolio while helping improve outcomes for patients around the world. As a Design Quality Engineer, you will partner with cross-functional teams to support sustaining engineering and lifecycle management activities, ensuring products continue to meet quality, regulatory, and business requirements. Before applying, please note that this position is not eligible for employer-sponsored immigration support. Applicants must be currently authorized to work in the United States and must not require S+N sponsorship now or in the future to maintain that authorization What will you be doing? • Support product lifecycle management activities, including design changes, product improvements, investigations, and quality plans. • Lead and support risk management activities, including risk assessments, FMEAs, implementation of risk controls, and effectiveness reviews. • Review and approve design verification and validation activities, manufacturing process changes, supplier qualifications, and process validations. • Investigate complaints, nonconformances, CAPAs, post-market surveillance trends, and product risk assessments to identify root causes and drive corrective actions. • Ensure compliance with Design Controls, Change Control, Risk Management, and Quality System requirements throughout the product lifecycle. • Collaborate with Regulatory Affairs, R&D, Manufacturing, Operations, Clinical, Marketing, and Supplier Quality teams to support product quality and regulatory compliance. • Provide technical quality guidance and influence decisions that impact product performance, compliance, and patient safety. • Drive continuous improvement initiatives using quality metrics, post-market data, and operational performance insights. What will you need to be successful? Required Qualifications • Bachelor of Science degree in Engineering or a related technical discipline. • Minimum of 2 years of experience in the medical device industry or another regulated environment. • Working knowledge of: FDA Quality System Regulations (QSR) ISO 13485 ISO 14971 Design Controls Risk Management methodologies CAPA and complaint handling processes • Strong analytical, communication, collaboration, and problem-solving skills. • Ability to develop and implement solutions to complex quality challenges. Preferred Qualifications • Certified Quality Engineer (CQE). • Six Sigma certification. • Experience supporting sustaining engineering and product lifecycle management. • Experience participating in audits, inspections, and regulatory submissions. Physical Demands • Primarily seated work with occasional light lifting. Travel Requirements • Less than 10% travel. The anticipated base compensation range for this position is $74,250 to $111,500 USD annually. The actual base pay offered to the successful candidate will be based on multiple factors, including but not limited to job-related knowledge/skills, experience, geographical location, and internal equity. It is not typical for an individual to be hired at the high end of the range for their role at Smith + Nephew. In addition to base pay, we offer competitive bonus and benefits, including medical, dental, and vision coverage, 401(k), tuition reimbursement, medical leave programs, parental leave, generous PTO, paid company holidays, 8 hours of volunteer time annually, and a variety of wellness offerings such as EAP. #LI-HYBRID #LI-MA1