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Technical Writer - IV
Technical Writer - IVThe Fountain Group • Irving, TX
Technical Writer - IV

Technical Writer - IV

The Fountain Group • Irving, TX
[job_card.30_days_ago]
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  • [job_card.full_time]
[job_card.job_description]

Technical Writer – Medical Device Industry

Pay: $50–$57/hr
Duration: 6 months (Potential to extend)
Location: Onsite in Irving, TX


About the Role:

We are seeking an experienced Technical Writer to develop and manage technical documentation for products in a medical device or healthcare-regulated environment. This role supports cross-functional teams including R&D, Quality Assurance, and Process Owners to ensure documentation accuracy, clarity, and compliance with regulatory standards.


Key Responsibilities:

  • Develop and maintain a variety of technical documents including forms, procedures, test instructions, regulatory documents, and internal SOPs.
  • Translate complex technical content into clear, concise, and user-friendly materials for both technical and non-technical audiences (e.g., technicians, engineers).
  • Collaborate with cross-functional teams to gather, verify, and clarify information.
  • Ensure documentation aligns with applicable regulatory requirements and internal policies.
  • Manage document version control and maintain organized documentation archives.
  • Support risk assessments and usability studies to inform documentation strategies.
  • Assist in the creation of training materials and procedural guides.


Required Qualifications:

  • Bachelor’s degree in English, Communications, Life Sciences, Engineering, or equivalent field/experience.
  • 5+ years of technical writing experience, preferably within medical devices or healthcare. (Pharma, aerospace, or aviation backgrounds also considered.)
  • Strong understanding of medical terminology, regulatory documentation standards, and Good Documentation Practices (GDP).
  • Proficiency in Microsoft Office and document management systems.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple projects and meet tight deadlines.

Preferred Experience:

  • FDA-regulated environment
  • CAPA (Corrective and Preventive Actions) familiarity
  • Prior experience supporting regulated documentation in medical devices or pharma

#LI-BE1
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Technical Writer IV • Irving, TX

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