Technical Writer

Unicon Pharma Inc; United States; Remote; USD 70,000 - 151,000; Part time

Job summary

Unicon Pharma Inc seeks a Technical Writer III (Contractor) to focus on policy and SOP development for AI governance and lifecycle. The role, part-time and remote, involves drafting procedural documents and ensuring compliance with style guides. The ideal candidate should have substantial experience in technical writing and a master's degree.

Qualifications

• 5+ years of technical/medical writing experience
• Ability to manage multiple concurrent writing projects
• Familiarity with AI regulations preferred

Responsibilities

• Draft procedural documents based on outlines and SME input
• Incorporate reviewer feedback and manage document versions
• Perform high-quality copy editing

Skills

Technical/Medical Writing

Attention to Detail

Document Management

Education

Master’s or Graduate-level Education

Tools

Veeva

SharePoint

Job description

Direct message the job poster from Unicon Pharma Inc

Senior Pharma Recruiter at Unicon Pharma

Role Overview:

• Title: Technical Writer III (Contractor)
• Location: Remote (U.S.-based)
• Department: CDS Bridge Process Development
• Workload: 12–24 hours/week through September 2025
• Focus Area: Policy and SOP development for AI governance and lifecycle
• Client: Leading biotech/pharma company (via EDSC – Enterprise Data Science Council)

Primary Responsibilities:

• Draft procedural documents from outlines and SME input
• Incorporate and reconcile reviewer feedback
• Lead comment reconciliation meetings across cross-functional teams
• Track and manage document versions, feedback, and timelines
• Perform high-quality copy editing (grammar, syntax, formatting)
• Ensure clarity, consistency, and compliance with style guides

Required Skills:

• 5+ years of technical/medical writing experience (esp. GxP, SOPs, policies)
• Ability to manage multiple concurrent writing projects
• High attention to accuracy and detail

Preferred Skills:

• Familiarity with AI regulations (EU AI Act, Colorado AI Act)
• Knowledge of AI governance frameworks (e.g., NIST AI RMF)
• Understanding of data privacy laws and drug development processes
• Experience with document management systems (e.g., Veeva, SharePoint)
• Certifications like BELS, AMWA, or in procedural/data science writing

Education:

• Preferred: Master’s or graduate-level education
• Work directly with senior enterprise leaders to finalize one AI policy and one AI SOP
• Be part of shaping enterprise-wide AI governance documentation
• Drafting support includes an existing policy draft and SOP process map/outline

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Writing/Editing

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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