Quality Manufacturing Technical Writer

Job Summary

Working remotely on a full-time basis, the Quality Manufacturing Technical Writer will develop and maintain documentation for various pharma manufacturing workstreams, focusing on contamination control, manufacturing controls, data integrity, quality systems, and laboratory controls.

Key responsibilities

• Create and manage technical documentation related to contamination control and environmental monitoring
• Ensure compliance with manufacturing and production controls through accurate documentation
• Support data integrity and governance initiatives by developing relevant technical materials

Required qualifications

• Experience in technical writing within the pharmaceutical or biotech industries
• Knowledge of regulatory standards and quality systems in manufacturing
• Familiarity with data integrity and governance practices
• Understanding of contamination control and environmental monitoring processes
• Ability to work independently in a remote setting while collaborating with cross-functional teams