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Boston Scientific Technical Writer II 
Costa Rica 
667509033

04.05.2025

Costa Rica-Heredia

Hybrid Roles:

Your Responsibilities Include:

  • Documentation Creation and Maintenance: Develop and maintain design history files (DHF), risk management file deliverables (e.g., Hazard Analysis, DFMEA), and other technical documents for interventional cardiology medical devices.
  • Quality System and Regulatory Compliance: Help ensure that all documentation complies with:
    • Relevant Boston Scientific Quality System requirements and good documentation practices (GDP).
    • Relevant regulatory standards (e.g., FDA, ISO), and other global medical device regulations (e.g., MDR).
  • Content Management: Manage the release and revision of version-controlled documents in the BSC document management system.
  • Collaboration: Work closely with cross-functional teams including Regulatory Affairs, Research & Development, and Clinical Risk to gather information and ensure accuracy of technical content.
  • Editing and Proofreading: Review and edit documentation for clarity, grammar, and style, ensuring consistency across all materials. Incorporate feedback from stakeholders to continuously improve documentation quality and usability.

What we're looking for:

  • Education: Bachelor's degree in Technical Writing, English, Communications, Engineering, or a related field.
  • Experience: Minimum of 2 years of experience in technical writing, preferably in the medical device industry.
  • Language: Must be bilingual in Spanish and English with a strong command of the English language.
  • Skills:
    • Excellent writing, editing, and proofreading skills.
    • Ability to manage multiple projects and meet deadlines.
    • Proficiency in document management systems and content creation tools.
    • Strong interpersonal and communication skills.
    • Attention to detail and a commitment to producing high-quality documentation.
Preferred Qualifications:
  • Previous experience working in a regulated environment.
  • Working knowledge of medical device regulations and standards.
  • Knowledge of medical terminology and clinical practices.