Quality Manufacturing Technical Writer (Pharma)

TL;DR

Quality Manufacturing Technical Writer (Pharma): Developing technical documentation for pharmaceutical manufacturing processes with an accent on quality systems, data integrity, and regulatory compliance. Focus on creating high-quality technical content for specific workstreams including contamination control, facilities, and laboratory controls.

Location: Must be based in the United States. Remote work is supported, with hybrid collaboration encouraged for those near office locations.

Company

hirify.global is a consulting firm providing regulatory, quality, and compliance expertise to biotech, med device, and pharmaceutical organizations to accelerate the introduction of new therapies.

What you will do

• Create and manage technical documentation for pharmaceutical manufacturing workstreams.
• Develop content for Contamination Control and Environmental Monitoring.
• Write and review documentation for Manufacturing and Production Controls.
• Establish documentation for Data Integrity and Data Governance.
• Support documentation needs for Facilities, Utilities, and Quality Systems.
• Produce technical content for Laboratory Controls.

Requirements

• Location: Must be based in the United States.
• Professional experience in technical writing specifically for pharma manufacturing.
• Ability to work remotely or on a hybrid basis if living near a company office.

Culture & Benefits

• Commitment to diversity, equity, and inclusion, fostering an authentic workplace.
• Collaborative and entrepreneurial environment that encourages innovation.
• Flexible remote work policy with opportunities for in-person collaboration.
• Transparent hiring process with personal application reviews and guaranteed outcome notifications.