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Technical Writer

Intellectt Inc

Irving (TX)

On-site

USD 80,000 - 145,000

Full time

2 days ago
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Job summary

A leading company in the medical equipment manufacturing sector seeks a skilled Technical Writer to develop and maintain comprehensive technical documentation. You will translate complex information into user-friendly content, ensuring compliance and collaboration with various teams. This role, requiring a bachelor's degree and 5+ years of experience in technical writing, offers a competitive salary in the Dallas area.

Qualifications

  • 5+ years of technical writing experience, especially in the medical device or healthcare industry.
  • Strong understanding of medical terminology and regulatory requirements.
  • Bachelor’s degree or equivalent background in Tech Writing.

Responsibilities

  • Develop and maintain technical documentation including forms and regulatory documents.
  • Translate complex technical information into clear content for various audiences.
  • Collaborate with teams to ensure documentation accuracy and compliance.

Skills

Medical terminology understanding
Document management systems proficiency
Good Documentation Practices familiarity
Excellent written communication skills
Excellent verbal communication skills
Project management ability

Education

Bachelor’s degree in English, Communications, Life Sciences, Engineering

Tools

Microsoft Office

Job description

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• Develop and maintain technical documentation including forms, procedures, instructions for testing products, and regulatory documents.

• Translate complex technical information into clear, concise, and user-friendly content for various audiences including technicians and engineers.

• Collaborate with cross-functional teams including R&D, Quality Assurance and Process Owners to gather information and ensure accuracy.

• Ensure all documentation complies with applicable internal policy standards.

• Manage document version control and maintain documentation archives.

• Participate in risk assessments and usability studies to inform documentation strategy.

• Support the creation of training materials and internal SOPs.

Experience: 5+ years of experience in technical writing, preferably in the medical device or healthcare industry.

Key Skills:

• Strong understanding of medical terminology and regulatory requirements.

• Proficiency in document management systems and Microsoft Office.

• Familiarity with Good Documentation Practices (GDP) and regulatory processes.

• Excellent written and verbal communication skills.

• Ability to manage multiple projects and meet tight deadlines.

Preferred Experience: Medical Device background, FDA Regulated, Pharma, CAPA

Education: Bachelor’s degree in English, Communications, Life Sciences, Engineering, or equivalent background and experience in Tech Writing. (background & experience)

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Information Technology
  • Industries
    Medical Equipment Manufacturing and Medical Practices

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