Technical Writer

Actalent - Hollywood, FL

Full-time - Entry Level

Hollywood, FL

10,001+ employees

Administrative and Support Services

About the position

The Technical Writer - Global Quality & Compliance is responsible for creating, revising, and managing global quality documentation, including Standard Operating Procedures (SOPs), policies, and the Global Quality Manual. This role supports global and site quality initiatives, ensuring compliance with regulatory standards and internal requirements.

Responsibilities

• Author and manage global SOPs and policies.
• Update the Global Quality Manual and Policy.
• Collaborate with SMEs for accurate, compliant documentation.
• Support quality initiatives with clear, precise documentation.
• Ensure timely updates and distribution of documents.
• Implement changes in the document management system.
• Maintain consistent documentation practices across sites.
• Participate in document reviews and approval processes.
• Recommend improvements to documentation processes.
• Support audits with organized documentation and follow-ups.

Requirements

• 2+ years Technical Writing experience
• Experience with Document Management
• Knowledge of Quality Systems and SOPs
• Bachelor's Degree

Nice-to-haves

• Experience in Regulatory Affairs
• Familiarity with FDA regulations
• Knowledge of cGMP in Pharmaceuticals or Medical Device industry