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Senior Technical Writer

Meet Life Sciences

United States

On-site

USD 63,000 - 83,000

Full time

Yesterday
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Job summary

A leading company in biotechnology research is seeking a Senior Technical Writer to enhance accessibility and documentation within their UX team. The ideal candidate will possess strong writing and editing skills, with experience in the medical device industry. Responsibilities include creating technical documents, managing UX strings, and collaborating with cross-functional teams. This role offers a chance to guide and mentor other writers while improving documentation processes.

Benefits

Medical insurance
Vision insurance
401(k)

Qualifications

  • 5-7 years of relevant experience or BA/BS in related field.
  • Minimum 3 years writing/editing in the medical device industry.
  • Experience in healthcare or life sciences preferred.

Responsibilities

  • Create accessible text and technical microcopy within design files.
  • Manage UX strings across products for localization.
  • Lead improvements in documentation processes and tools.

Skills

Writing
Editing
Project Management
Collaboration
Attention to Detail
Storytelling

Education

BA/BS in Technical Writing
BA/BS in English

Tools

Microsoft Office
Figma
Jira
Confluence
Smartsheet
PLM (Arena, Polarian)

Job description

Position: Senior Technical Writer – UX Team

Overview:

We are seeking a Senior Technical Writer to support accessibility, localization, and documentation efforts within our UX team. You will manage and create accessibility annotations, UX strings, and technical documentation, collaborating closely with cross-functional teams across global locations. Strong writing, editing, and organizational skills are essential.

Key Responsibilities:

  • Create accessible text and technical microcopy (e.g., string IDs) within design files.
  • Manage UX strings across products to support localization.
  • Write clear, concise design/technical documents for regulatory and quality processes.
  • Submit and maintain documents in Product Lifecycle Management (PLM) systems.
  • Lead improvements in documentation processes and tools.
  • Guide and mentor other Technical Writers; review and document content decisions.
  • Maintain Technical Writing guidelines within UX style standards.
  • Collaborate with stakeholders and UX managers to align content outputs and deadlines.

Requirements:

  • BA/BS in Technical Writing, English, or related field, or 5–7 years of relevant experience.
  • Minimum 3 years writing/editing in the medical device industry.
  • UX-Focused Technical Writing (MUST HAVE)
  • Experience in healthcare, life sciences, or diabetes (preferred).
  • Strong grasp of medical and technical content.

Skills & Tools:

  • Exceptional writing/editing for lay audiences; attention to detail.
  • Ability to communicate complex concepts clearly; strong storytelling skills.
  • Familiarity with design tools and UX processes.
  • Strong project management, multitasking, and leadership abilities.
  • Skilled in Microsoft Office; experience with PLM (Arena, Polarian), Figma, Miro, Jira, Confluence, Smartsheet (preferred).
  • Excellent interpersonal and collaboration skills in agile environments.
Seniority level
  • Seniority level
    Associate
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Research
  • Industries
    Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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