Technical Writer

We are seeking an experienced Technical Writer to support quality system and technical documentation in a regulated (GxP) environment. This role requires strong technical writing expertise—not content or marketing writing—and a proven ability to develop, review, and manage controlled documents with accuracy and consistency.

• Deliver high-quality, error-free technical documents that meet international standards of written English.
• Develop, revise, and maintain SOPs, work instructions, procedures, tools, and resource documents using approved templates and style guides.
• Edit documents for grammar, clarity, formatting, consistency, and technical accuracy.
• Ensure quality system documents are aligned, accurate, and consistent across related documentation.
• Collaborate with cross-functional teams and stakeholders to ensure timely document development and approvals.
• Facilitate the document review and approval process, reconcile reviewer comments, and resolve feedback efficiently.
• Support multiple documentation projects and document types simultaneously.
• Participate on project teams as required.
• Comply with HSE policies, maintaining a safe work environment and supporting site and corporate safety goals.

• Proven experience as a Technical Writer in a regulated or technical environment.
• Strong command of written English, including grammar, structure, and technical style.
• Hands-on experience with controlled documents and quality systems.
• Familiarity with technical writing standards, templates, and style guides.
• Strong organizational and stakeholder communication skills.

• Experience in Pharmaceutical, Biotech, or Medical Device industries.
• Knowledge of GMP, GxP, ISO, or QMS documentation.
• Experience using EDMS / document control systems.
• Contract or project-based documentation experience.