Technical Writer

Jobs via Dice; Irving (TX); On-site; USD 90,000 - 115,000; Full time

Job summary

A leading company in the healthcare sector is seeking a Technical Writer to create clear documentation supporting innovative projects. This mid-senior-level position will involve developing regulatory documents and collaborating with cross-functional teams to ensure information accuracy. Candidates should have strong writing skills, familiarity with medical terminology, and experience with document management systems.

Qualifications

• 5+ years of experience in technical writing, preferably in the medical device or healthcare sector.
• Strong understand of medical terminology and regulatory requirements.
• Ability to manage multiple projects and meet tight deadlines.

Responsibilities

• Develop and maintain technical documentation, including forms, procedures, and regulatory documents.
• Translate complex technical information into user-friendly content for diverse audiences.
• Collaborate with cross-functional teams to gather information and ensure accuracy in documentation.

Skills

Technical Writing

Medical Terminology

Document Management Systems

Microsoft Office

Communication

Education

Degree in English, Communications, Life Sciences, Engineering

Job description

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Dice is the leading career destination for tech experts at every stage of their careers. Our client, Horizontal Talent, is seeking the following. Apply via Dice today!

We are seeking a talented Technical Writer to join our dynamic team. This role offers the opportunity to create clear and concise documentation that supports our innovative projects in the healthcare industry.

Responsibilities

• Develop and maintain technical documentation, including forms, procedures, and regulatory documents.
• Translate complex technical information into user-friendly content for diverse audiences.
• Collaborate with cross-functional teams to gather information and ensure accuracy in documentation.
• Ensure compliance with internal policy standards and manage document version control.
• Participate in risk assessments and usability studies to inform documentation strategies.
• Support the creation of training materials and internal standard operating procedures (SOPs).
  
  

Skills

• 5+ years of experience in technical writing, preferably in the medical device or healthcare sector.
• Strong understanding of medical terminology and regulatory requirements.
• Proficiency in document management systems and Microsoft Office.
• Excellent written and verbal communication skills.
• Ability to manage multiple projects and meet tight deadlines.
  
  

Preferred Skills

• Experience in the medical device industry, particularly with FDA regulations.
• Familiarity with Good Documentation Practices (GDP) and regulatory processes.
• Background in English, Communications, Life Sciences, Engineering, or related fields.
  
  

We are committed to fostering a diverse, equitable, and inclusive workplace where all individuals feel valued and empowered to contribute their unique perspectives.

Once you apply for this position, you may receive a phone call, SMS or email at the time of application from our Virtual AI Recruiter, Alex, to conduct an initial interview.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Marketing, Public Relations, and Writing/Editing

• Industries

  Software Development

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