100% Remote - Senior Technical Writer (GxP & Pharma/Lifescience domain)

Jobs via Dice; United States; Remote; USD 103,000 - 121,000; Full time

Job summary

A leading company is seeking a Senior Technical Writer to work 100% remote in the pharmaceutical sector. The role involves drafting and editing procedural documents, ensuring clarity, compliance, and accuracy. Candidates should have extensive experience in technical writing and knowledge of industry regulations. The position requires strong attention to detail and the ability to manage multiple projects under tight deadlines.

Qualifications

• 5 years of experience in medical writing or technical writing required.
• Experience within a pharmaceutical or biotechnology organization preferred.
• Ability to handle multiple projects with high accuracy.

Responsibilities

• Contributes to efficient content authoring of procedural documents.
• Edits and incorporates reviewer comments.
• Manages multiple document updates and ensures compliance with style guides.

Skills

Detail-oriented work

Writing and editing

Communication skills

Proficiency with MS Word

Document management systems

Time management under deadlines

AI Regulation knowledge

Data privacy regulation knowledge

GxP knowledge

Education

5 years of relevant medical writing or technical writing experience

Tools

MS Word

MS Office

Job description

100% Remote - Senior Technical Writer (GxP & Pharma/Lifescience domain)

100% Remote - Senior Technical Writer (GxP & Pharma/Lifescience domain)

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

One of our direct Pharmaceutical client is looking to hire 100% Remote - Senior Technical Writer (GxP & Pharma/LifeScience domain).

Responsibilities:

• Once provided key messages in an outline and access to subject matter experts, significantly contributes toward efficient content authoring of draft procedural document text.
• Edits and incorporates reviewer comments in policy and procedural document.
• Triages reviewer comments and leads a comment reconciliation meeting to obtain alignment from the cross functional review team.
• Tracks feedback, review comments, and document updates. Communicates comment resolution to team.
• Ensures that policy and procedural document are clear, concise and technically accurate.
• Ensures consistency both within and between the policy and procedural document.
• Verifies accuracy of own work and ensures compliance to internal style guides and templates.
• Tracks and manages multiple concurrent document updates including statuses, timelines, and action items.
• Copy edits documents (including grammar, syntax, punctuation, style, clarity and formatting) to a high professional standard.
  
  

Knowledge and Skills:

• Ability to independently perform highly detail-oriented work in writing, reviewing and editing procedural documents with high degree of accuracy and efficiency.
• Strong proficiency with MS Word required, experience with document management systems and MS Office tools preferred.
• Demonstrates strong verbal, written, and interpersonal communication skills.
• Demonstrates ability to complete high quality work on multiple concurrent projects under tight deadlines.
• Knowledge of AI Regulation (e.g. European Union AI Act, Colorado AI Act) and AI Governance Frameworks (e.g National Institute of Standards and Technology AI Risk Management Framework) strongly preferred.
• Knowledge of data privacy regulation and frameworks strongly preferred.
• Knowledge of drug development processes or the GxP quality framework strongly preferred.
  
  

Education and Experience:

• 5 years of relevant medical writing or technical writing experience of policies, procedural documents, or other GxP documents required.
• Experience within a pharmaceutical/biotechnology organization, law firm, technology organization, or data science organization preferred.
  
  

Required Years of Experience: 5 years of relevant medical writing or technical writing experience of policies, procedural documents, or other GxP documents required.

Top 3 Required Skill Sets:

• Ability to independently perform highly detail-oriented work in writing, reviewing and editing procedural documents with high degree of accuracy and efficiency.
• Strong proficiency with MS Word required, experience with document management systems and MS Office tools preferred.
• Demonstrates ability to complete high quality work on multiple concurrent projects under tight deadlines.
  
  

Top 3 Nice to Have Skill Sets:

• Knowledge of AI Regulation (e.g. European Union AI Act, Colorado AI Act) and AI Governance Frameworks (e.g National Institute of Standards and Technology AI Risk Management Framework) strongly preferred.
• Experience writing or experience operationalizing data privacy policy or procedural documents strongly preferred.
• Board of Editors in the Life Sciences certification, American Medical Writers Association certification, or a certification related to procedural document writing or data science preferred.

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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