We are seeking an experienced Quality Assurance Engineer - Medical Devices to support quality engineering activities throughout the product development and manufacturing lifecycle. The ideal candidate will have strong experience in medical device quality, process verification and validation, Design/Process FMEA, Design Controls, risk management, and product testing.
Bachelor's degree in engineering, Science, or another relevant technical discipline.
5+ years of experience in the medical device industry, preferably in Quality Engineering or Quality Assurance.
Hands-on experience with Process Verification and Validation.
Experience with risk management, product testing, and quality problem-solving.
Conduct and support Process Verification and Process Validation (PV/PPQ) activities in accordance with established procedures and regulatory requirements.
Develop, review, and maintain Design FMEA (DFMEA) and Process FMEA (PFMEA) documentation.
Support Design Control activities throughout the product development lifecycle.
Perform product and process risk management and risk assessments.
Support product testing, verification, and validation activities and ensure appropriate documentation is completed.
Interpret engineering blueprints, drawings, GD&T, and technical specifications.
Participate in New Product Development (NPD) activities and provide quality engineering support from development through production implementation.
Support CAPA, nonconforming material, deviation, and corrective/preventive action processes.
Investigate quality issues using structured root-cause analysis and problem-solving methodologies.
Support compliance with applicable medical device quality and regulatory requirements.
Collaborate with manufacturing and onsite teams to ensure successful implementation of validated processes and quality requirements.
Work cross-functionally with Engineering, Manufacturing, R&D, Regulatory, Operations, and other stakeholders to resolve quality issues.
Participate in continuous improvement initiatives using Lean, Six Sigma, and other quality improvement methodologies.
Provide quality input and technical support to senior leadership on quality initiatives and improvement programs.
Manage multiple projects and priorities while meeting established timelines and quality objectives.
Prepare, review, and maintain quality documentation, reports, and technical records.
Numbers & Facts
Location
Boston, MA
Skills
Blueprintsunmatched
Continuous Improvementunmatched
Corrective Actionunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Cross-Functionalunmatched
Design Failure Mode and Effects Analysis (DFMEA)unmatched
Documentationunmatched
Engineering Drawingunmatched
Establish Prioritiesunmatched
Failure Mode and Effects Analysis (FMEA)unmatched
Geometric Dimensioning and Tolerancingunmatched
Healthcare Qualityunmatched
Leadershipunmatched
Lean Six Sigmaunmatched
Manufacturingunmatched
Medical Equipmentunmatched
Medical Office Administrationunmatched
Multitaskingunmatched
Problem Solving Skillsunmatched
Procedure Developmentunmatched
Process Failure Mode and Effects Analysis (PFMEA)unmatched
Process Managementunmatched
Process Validationunmatched
Product Developmentunmatched
Product Lifecycleunmatched
Product Supportunmatched
Product Testingunmatched
Project/Program Managementunmatched
Quality Assuranceunmatched
Quality Engineeringunmatched
Quality Managementunmatched
Regulationsunmatched
Regulatory Requirementsunmatched
Research & Development (R&D)unmatched
Risk Analysisunmatched
Risk Managementunmatched
Root Cause Analysisunmatched
Technical Supportunmatched
Time Managementunmatched
Validation Testingunmatched
🎯
Be found by employers
5,500+ employers search our resume database daily. Add yours to get found by recruiters looking for candidates like you.
Level up your application
Professional resume templates
Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.