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 environmentCAPA (Corrective and Preventive Actions) familiarityPrior experience supporting regulated documentation in medical devices or pharmaLI-BE1