Technical Writer

Schedule:

Monday–Friday, 8:00 AM – 5:00 PM

100% Onsite

6-Month Contract with High Likelihood of Extension/Conversion

$28/hour

We are seeking a detail-oriented Technical Documentation Writer to support ongoing documentation initiatives within a regulated pharmaceutical manufacturing environment. This is a traditional technical writing role focused on completing and improving controlled GMP documentation to ensure clarity, compliance, and operational efficiency.

This position offers strong potential for full-time conversion and is ideal for candidates looking to build long-term stability within a growing pharmaceutical organization.

• Author, revise, and finalize Standard Operating Procedures (SOPs), batch records, forms, and related GMP documentation.
• Ensure documents meet regulatory standards and align with internal quality systems.
• Collaborate with Manufacturing, Quality, and Compliance teams to gather technical information and translate it into clear, user-friendly documentation.
• Review existing procedures for accuracy, consistency, and compliance with current GMP requirements.
• Support documentation projects to ensure timely completion of deliverables.
• Maintain document control standards and support continuous improvement of documentation practices.
• Utilize electronic quality systems (including Track Wise, if applicable) to manage document workflows and change controls.

• Pharmaceutical GMP experience is REQUIRED.
• 1–3 years of technical writing experience in a regulated pharmaceutical or life sciences environment.
• Strong understanding of Good Manufacturing Practices (GMP) and quality documentation standards.
• Proven ability to write clear, structured, and compliant procedural documentation.
• Proficiency in Microsoft Office (especially Word) with experience formatting controlled templates.
• Strong organizational skills and ability to manage multiple documentation assignments simultaneously.
• Excellent written and verbal communication skills.

• Experience working with Track Wise quality management system (strong plus).
• Experience supporting manufacturing or aseptic operations documentation.

• High visibility role supporting critical GMP documentation initiatives.
• Opportunity to contribute directly to quality and compliance excellence within pharmaceutical manufacturing.