Senior Quality Engineer

Summary Seeking a Senior Quality Engineer with strong MDR remediation and medical device manufacturing quality experience to support compliance, validation, and risk management activities for regulated product families. Roles & Responsibilities Support MDR remediation and manufacturing quality assurance activities Develop and maintain PFMEAs, Control Plans, and risk management documentation Conduct First Article Inspections (FAIs), dimensional verification, and packaging evaluations Perform process validation activities including IQ, OQ, PQ, and test method validations Conduct production floor assessments and process observations to support risk evaluations Collaborate with Manufacturing, Quality, Warehouse, Planning, and Product Engineering teams Review and approve manufacturing change orders and MDR-related updates Support labeling verification, packaging testing, and technical documentation updates Maintain documentation and change records within Agile PLM Process validation and test method validation experience PFMEA, Control Plan, and risk management expertise Experience with FAIs, dimensional verification, and manufacturing changes Knowledge of FDA 21 CFR Part 820 and EU MDR (2017/745) Familiarity with ISO 13485, ISO 14971, and IEC 60601 Experience with change control and medical device quality systems Education & Experience Bachelor's degree in Engineering or related discipline 4+ years of relevant experience (MDR experience highly preferred) DOE/Minitab experience Computer System Validation (CSV) SOP development Agile PLM experience Packaging validation and fit testing #J-18808-Ljbffr Creative Solutions Services, LLC