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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