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

Jobs via Dice; United States; Remote; USD 75,000 - 151,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Senior Technical Writer to join their remote team. This role involves authoring, reviewing, and editing policy and procedural documents while ensuring adherence to regulatory and compliance standards. Ideal candidates will have extensive experience in medical or technical writing, with a focus on GxP environments. If you excel in detail-oriented work and enjoy managing several projects simultaneously, this could be a fantastic next step in your career.

Qualifications

• 5 years of relevant medical writing or technical writing experience required.
• Experience within a pharmaceutical or biotechnology organization preferred.

Responsibilities

• Contributes to efficient content authoring of procedural documents.
• Tracks and manages multiple concurrent document updates.
• Ensures clarity and technical accuracy of documents.

Skills

Detail-oriented work

Strong proficiency with MS Word

Strong verbal and written communication skills

Education

5 years of relevant medical writing or technical writing experience

Job description

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

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

2 days ago Be among the first 25 applicants

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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