Senior Design Quality Engineer

Katalyst Healthcares & Life Sciences

Raynham, MA

JOB DETAILS
SKILLS
Analysis Skills, Biomedical Engineering, Blueprints, Change Control, Communication Skills, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Design Verification, Documentation, Engineering, FDA (Food and Drug Administration), Failure Mode and Effects Analysis (FMEA), Geometric Dimensioning and Tolerancing, ISO (International Organization for Standardization), Leadership, Lean Manufacturing, Lean Six Sigma, Maintain Compliance, Manufacturing Requirements, Marketing, Mechanical Engineering, Medical Equipment, Multitasking, Problem Solving Skills, Process Improvement, Process Validation, Product Development, Product Lifecycle, Product Lifecycle Management, Product Support, Quality Engineering, Quality Metrics, Regulations, Regulatory Compliance, Regulatory Requirements, Research & Development (R&D), Risk Management, Team Player, Technical Leadership, Technical/Engineering Design, Validation Testing
LOCATION
Raynham, MA
POSTED
1 day ago
Job Summary:
  • The Senior Design Quality Engineer will support product lifecycle management activities for medical devices by providing quality engineering leadership for design and process changes, risk management, verification and validation activities, and compliance with medical device regulations.
  • The role requires close collaboration with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, Marketing, and Operations.
Roles & Responsibilities:
  • Support design changes and process improvements throughout the product lifecycle.
  • Lead and execute Design Verification & Validation (V&V) activities.
  • Conduct Design FMEA and Process FMEA to identify and mitigate product and process risks.
  • Ensure compliance with Design Controls and applicable medical device regulations.
  • Collaborate with R&D, Manufacturing, Regulatory Affairs, and Marketing teams to support product development and sustaining engineering initiatives.
  • Drive risk management activities and support change control processes.
  • Participate in corrective and preventive action (CAPA) investigations and implementation.
  • Support nonconforming material investigations and quality system improvements.
  • Review and approve engineering documentation, protocols, reports, and design history files.
  • Provide technical leadership for quality engineering projects and continuous improvement initiatives.
  • Ensure compliance with applicable quality standards and regulatory requirements.
Education & Experience:
  • Bachelor's Degree in Engineering, Science, or a related technical discipline.
  • 5+ years of experience in the Medical Device industry.
  • Experience performing Process Verification and Validation activities.
  • Experience conducting Design FMEA and/or Process FMEA.
  • Strong knowledge of Design Controls and Quality Systems.
  • Excellent problem-solving, analytical, and decision-making skills.
  • Strong communication and cross-functional collaboration skills.
  • Ability to manage multiple priorities and lead technical projects.
  • Advanced degree (MS or higher) preferred.
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or related discipline preferred.
  • Experience in New Product Development (NPD).
  • Strong understanding of blueprint reading, inspection methods, and GD&T.
  • Experience with Design Excellence, Lean Manufacturing, and Six Sigma methodologies.
  • Medical device lifecycle management experience.
  • Knowledge of FDA, ISO 13485, and risk management standards.

About the Company

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Katalyst Healthcares & Life Sciences