Save Job Back to Search Job Description Summary Similar JobsJoin a cutting-edge medical technology environmentLead and support design quality activities across product development projects.About Our ClientThis organization is a rapidly expanding medical‑technology innovator focused on developing life‑changing therapeutic solutions. Its teams are united by a shared purpose and a passion for engineering excellence. The culture encourages creativity, cross‑functional collaboration, and continuous learning. Employees thrive in a supportive, mission‑oriented environment designed to empower bold ideas. The company is committed to growth, inclusivity, and delivering meaningful impact to patients worldwide.Job DescriptionLead and support design quality activities across product development projects.Ensure compliance with applicable regulatory standards (FDA, ISO 13485, etc.).Drive design controls, including risk management, verification, and validation.Partner with R&D to identify and mitigate product and process risks early.Review and approve design documentation, specifications, and change controls.Support audits, inspections, and continuous improvement initiatives.Analyze quality data and implement corrective and preventive actions (CAPA).Provide guidance on quality best practices to cross-functional teams.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.The Successful ApplicantBachelor's degree in Engineering or related technical discipline (required).Extensive experience in design quality within the medical device industry.Strong knowledge of design controls, risk management (ISO 14971), and validation processes.Familiarity with FDA regulations and quality standards such as ISO 13485.Proven ability to work cross-functionally with engineering and regulatory teams.Strong analytical, problem-solving, and communication skills.Experience supporting audits and regulatory submissions is highly desirable.What's on OfferCompetitive salary and performance-based incentives.Comprehensive benefits package including healthcare and retirement plans.Opportunity to work on innovative, meaningful medical technologies.A collaborative and supportive working environment.Career progression opportunities within a growing organization.Exposure to end-to-end product development in a regulated setting.ContactConnor ColomboQuote job refJN-062026-7037697Job summarySectorLife SciencesSub SectorMedical devicesIndustryIndustrial / ManufacturingLocationCherry HillContract TypePermanentConsultant nameConnor ColomboJob ReferenceJN-062026-7037697
