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Quality Engineer

Commonwealth Sciences

Quality Assurance Engineer

Position located in Boston, MA

Responsibilities:
  • Provide quality oversight and support for combination product development and commercialization activities.
  • Maintain and support the Quality Management System (QMS) in compliance with ISO 13485, 21 CFR Part 820, 21 CFR Part 4, and other applicable FDA and international regulations.
  • Partner with R&D, Engineering, Manufacturing, Regulatory, and Clinical teams to ensure quality requirements are incorporated throughout the product lifecycle.
  • Support Design Control activities, including Design History File (DHF) documentation, design reviews, design verification and validation, and design changes.
  • Assist with risk management activities, including product risk assessments, FMEAs, and implementation of risk controls.
  • Review and approve quality and technical documentation, specifications, protocols, reports, and change controls.
  • Support investigation of nonconformances, deviations, complaints, and CAPAs, including root-cause analysis and effectiveness checks.
  • Participate in supplier qualification, supplier quality activities, and oversight of external manufacturing partners.
  • Support internal and external audits and assist with preparation of responses to audit findings.
  • Provide quality guidance to cross-functional project teams and help identify potential compliance risks early in the development process.
  • Contribute to continuous improvement initiatives related to product quality, processes, and the overall QMS.
Requirements:
  • Bachelor's degree in Engineering, Life Sciences, Quality, or a related technical field.
  • 3+ years of experience in Quality Engineering within medical device, pharmaceutical, biotechnology, or combination product environments.
  • Working knowledge of ISO 13485, FDA 21 CFR 820, and 21 CFR Part 4.
  • Experience with Design Controls, risk management, CAPA, nonconformance investigations, and change control.
  • Experience working in a regulated GMP environment preferred.
  • Strong technical writing, documentation, problem-solving, and communication skills.
  • Ability to work effectively with cross-functional teams in a fast-paced product development environment.
Vacancy posted 3 days ago
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