Job Description

Responsibilities

  • Provide escalation support for significant quality issues
  • Ensure timely assessment and containment of quality event
  • Participate in MRB activities, ensuring consistent, compliant, and risk-based disposition of nonconforming material
  • Own and oversee quality input to post-release design and process changes (ECOs, deviations, waivers, temporary changes)
  • Ensure thorough change impact assessments are performed to determine verification, validation, revalidation, and documentation requirements
  • Ensure appropriate risk controls, benefit-risk justifications, and verification activities are implemented and documented
  • Ensure sustained compliance with applicable regulations and standards, including ISO 13485, FDA 21 CFR 820 (QSR), EU MDR (as applicable), and relevant IEC standards (e.g., IEC 60601-1)
  • Collaborating with Supplier Quality and Supply Chain leadership on supplier-related quality issues

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