Position: Technical Writer – Pharma/Biotech

Location: Raleigh, North Carolina - 100% Onsite

Long Term contract on W2/1099

**No C2C**

We are seeking a highly skilled Technical Writer with experience in the Pharma/Biotech industry to support documentation needs for a greenfield project. This role requires strong technical knowledge, organizational skills, and the ability to effectively collaborate with stakeholders to ensure high-quality documentation and adherence to project timelines.

Key Responsibilities:

• Provide expert guidance on the writing process, ensuring clarity in document type selection, structure, style, and language for operational documents.
• Actively engage with stakeholders to ensure project schedule milestones are met in line with client requirements.
• Demonstrate technical knowledge in at least one of the following areas: Utilities Equipment, Maintenance Processes, Preventive Maintenance Plans, Reliability, MRO Spare Parts Management, or Facilities/Utilities/Production Maintenance.
• Lead administrative processes related to documentation, acting as a liaison between area engineers, process subject matter experts (SMEs), and operational readiness teams.
• Provide regular progress reports on documentation creation.
• Develop and maintain strong relationships with internal and external stakeholders.
• Support document revisions through change control processes, ensuring standards are up to date.
• Process and manage documents using SAP, VeevaVault, and other document management tools.
• Ensure compliance with GMP, safety, and environmental standards throughout the construction site.
• Perform additional duties as assigned.

Qualifications:

• Proven expertise with Utilities Systems, SAP, and VeevaVault.
• Experience with GxP operations and pharmaceutical manufacturing.
• Strong proficiency in MS Word, Excel, and Adobe best practices.
• Excellent communication, organizational, and conflict resolution skills.
• Ability to read, write, and understand complex product documentation and standard operating procedures (SOPs).
• Experience in change management and thriving in a fast-paced, greenfield project environment.

If you are detail-oriented and passionate about contributing to innovative life sciences projects, we encourage you to apply!

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