Role:Quality Engineer Location:Westford, MA (100% Onsite) Experience Required: 25 years of Quality Engineering experienceExperience in Medical Device Manufacturing preferredPharma or Electronics industry candidates (regulated environment) are also acceptableKey Responsibilities: Support post-market quality engineering activities for medical devicesMaintain risk documentation and support risk reviewsPerform complaint investigations and failure analysisManage CAPA (Corrective and Preventive Action