
Senior Design Quality Engineer
Required skills
- FDA QSR
- ISO 13485
- ISO 14971
- risk management
- change control
- CAPA
- validation
- product lifecycle management
- quality system requirements
- regulatory submissions
Nice to have
- CQE
- Six Sigma
Role summary
Smith+Nephew is seeking a Senior Design Quality Engineer in Mansfield, MA, to support the lifecycle management of Sports Medicine Joint Repair products. This role ensures product safety, effectiveness, and compliance by leading risk management, design controls, validation activities, and investigations. The engineer will collaborate with cross-functional teams, provide quality oversight, and drive continuous improvement initiatives. A Bachelor's degree in Engineering and 5+ years of experience in a regulated industry, with strong knowledge of FDA QSR, ISO 13485, and ISO 14971, are required. Preferred qualifications include CQE or Six Sigma certification.
What will you be doing?
- Serve as the Design Quality representative for product support and lifecycle management activities, including product improvements, design changes, quality planning, investigations, and continuous quality enhancement initiatives
- Lead risk management activities including risk assessments, FMEA development and maintenance, implementation of risk controls, risk reviews, and verification of effectiveness
- Provide design quality oversight and approval for design verification and validation activities, sterilization validations, process validations, supplier qualifications, manufacturing process changes, and test methods
- Lead or support investigations related to complaints, nonconformances, CAPAs, post market surveillance, trend analysis, and product risk assessments to identify root causes and drive corrective and preventive actions
- Review and approve quality and engineering documentation to ensure compliance with design controls, change control, risk management, and quality system requirements
- Partner closely with Regulatory Affairs, Operations, R&D, Manufacturing, Marketing, Clinical, and Supplier Quality teams to support regulatory submissions, audits, inspections, and ongoing product support
- Act as a quality engineering resource for complex technical and compliance related issues, providing guidance and influencing decisions that impact product quality, patient safety, and business objectives
- Identify and drive continuous improvement opportunities through analysis of quality data, product feedback, risk management outputs, and operational performance metrics
- Provide technical leadership, training, guidance, and mentorship to support effective decision making, accountability, compliance, and quality excellence
What will you need to be successful?
- Bachelor of Science degree in Engineering or a technically related field
- 5+ years of experience in the medical device industry or another highly regulated environment
- Strong knowledge of FDA QSR, ISO 13485, and ISO 14971 requirements
- Experience with risk management, design controls, change control, CAPA, validation activities, and product lifecycle management
- Demonstrated ability to solve complex quality challenges and influence cross functional stakeholders
- Excellent communication, collaboration, and problem solving skills
- CQE and/or Six Sigma certification preferred
Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
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