Job Description


Responsibilities:
  • Draft, update, and optimize QMS procedures to align with Code beamer upgrades, organizational standards, and regulatory requirements.
  • Collaborate with cross-functional Quality and R&D teams to ensure procedures accurately reflect best practices and compliance expectations.
  • Translate technical and regulatory requirements into clear, practical documentation for end users.
  • Support change management processes, ensuring procedural updates are properly controlled and communicated.
  • Ensure documentation is compliant with ISO , CFR Part , EU MDR, and internal quality system standards.
  • Partner with stakeholders to validate that documentation aligns with both product development processes and regulatory needs.
    • Requirements:
  • Proven experience in the medical device industry, with strong knowledge of QMS documentation and procedures.
  • Hands-on experience authoring and revising procedures compliant ...

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