Contract Technical Writer

Location: Raleigh, NC (On-site)

Pay Rate: $40–$47/hour

Schedule: Monday-Friday 8am-5pmDuration: Initial 6–8 weeks with strong potential for extension

Openings: 2Overview

Responsibilities: Revise and update Standard Operating Procedures (SOPs) to support CAPA closure activities. Author, revise, and format technical documentation, including batch records and laboratory forms. Translate input from Quality, Manufacturing, and Laboratory subject matter experts into clear, compliant documentation. Ensure all documents comply with cGMP requirements and internal quality systems. Track assigned documentation against project timelines and CAPA due dates. Collaborate with cross-functional teams to verify technical accuracy before document approval. Utilize electronic document management and change control systems to draft, route, and maintain documentation.

Qualifications: Bachelor's degree in a scientific, technical, engineering, or communications-related field preferred; equivalent regulated manufacturing experience will be considered.3+ years of technical writing experience in a GMP-regulated pharmaceutical, biotech, medical device, or similar manufacturing environment. Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. Working knowledge of CAPA processes, document control, and quality management systems. Strong technical writing skills with an emphasis on clarity, consistency, and regulatory compliance. Ability to work independently in a fast-paced, deadline-driven environment. Proficiency with Microsoft Office and electronic document management systems. Position Details3–4 contract openings available immediately. Initial project expected to last 6–8 weeks, with a strong possibility of extension based on ongoing documentation needs. This is a fully on-site position in Raleigh, NC.