Senior Quality Engineer- Medical Device- Mount Laurel, NJ

• Serve as the quality representative on cross-functional product development initiatives, ensuring compliance with established quality system requirements throughout the product lifecycle.
• Partner with engineering teams to support design and development activities, including design reviews, documentation oversight, and phase-gate deliverables.
• Lead risk management efforts for new and existing products, including assessments, mitigation planning, documentation, and ongoing risk evaluations.
• Review and approve design changes, technical documentation, and engineering modifications to ensure alignment with quality and regulatory expectations.
• Support verification, validation, and product realization activities by assessing protocols, reports, and associated documentation for accuracy and completeness.
• Investigate quality issues, nonconformances, and customer-related concerns, driving corrective and preventive actions through effective root-cause analysis.
• Contribute to the development, maintenance, and continuous improvement of quality management system processes, procedures, and training materials.
• Provide technical leadership on quality and regulatory requirements while collaborating with internal stakeholders, suppliers, and external partners to support successful product commercialization.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.