Technical Writer

Job Summary

Supporting a biopharma client, the remote contract Technical Writer will distill technical information into high-quality written deliverables for regulatory submissions, ensuring compliance with health authority standards and timelines.

Key Responsibilities

• Distill technical information into concise written deliverables for regulatory submissions
• Read and synthesize technical documentation related to product development and testing
• Develop narratives, diagrams, tables, and figures while maintaining awareness of health authority regulations

Required Qualifications

• A minimum of 2-3 years of experience as a technical writer, preferably in the biopharma industry
• Experience with Good Manufacturing Practices (GMP) and documentation standards
• Knowledge of quality and technology transfer processes