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Technical Writer - IV

Technical Writer - IV

The Fountain GroupIrving, TX
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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
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    Technical Writer • Irving, TX