Medical Device Documentation Specialist

2 weeks ago

Limerick, Limerick, Ireland beBeeRegulated Full time €60,000 - €75,000

Document Development Specialist

A company based in Ireland is recruiting a skilled Document Development Specialist to join their team.

Key Responsibilities:

  • Create comprehensive technical and regulatory documents throughout the device lifecycle.
  • Collaborate with cross-functional teams to gather content.
  • Ensure documentation follows internal templates and regulatory standards.
  • Participate in content reviews and implement stakeholder feedback.
  • Organize deliverables and track completion milestones across the documentation suite.

Requirements:

  • Strong knowledge of FDA, EU MDR, ISO 13485, and ISO 14971 documentation standards.
  • Proficiency with document authoring tools such as Microsoft Word.
  • Experience working on Class II or III medical devices.
  • Excellent collaboration and communication skills.
  • Able to work independently and manage priorities.

What We're Looking For:

  • Technical writing expertise in regulated industries.
  • Document authoring skills using MS Word.
  • Knowledge of medical device regulations (FDA, EU MDR, ISO).
  • Excellent collaboration and communication skills.

Why It's a Great Opportunity:

  • Join a dynamic team dedicated to delivering high-quality medical devices.
  • Contribute to the development of life-changing products.
  • Enjoy a supportive work environment that fosters growth and learning.

Benefits:

  • Competitive compensation package.
  • Comprehensive benefits program.
  • Opportunities for professional development and advancement.

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