Technical Writer

Duration: 18 month contract (potential of extension)

We are seeking a skilled Technical Writer to support documentation needs within a highly regulated pharmaceutical environment. This role focuses on creating clear, accurate, and compliant technical documents used across manufacturing, laboratory, and engineering operations.

• Develop, edit, and maintain technical documents including SOPs, protocols, reports, work instructions, and required operational tools.
• Collaborate closely with subject matter experts (SMEs) to gather information and ensure accuracy, clarity, and scientific credibility.
• Ensure all documentation meets company standards, regulatory expectations, and industry guidelines.
• Support document revisions and version control processes within the organization.
• Help standardize document structure, formatting, tone, and compliance across teams.

• Prior experience as a Technical Writer in pharma, biotech, medical device, or another regulated industry.
• Strong understanding of GMP/GxP documentation practices.
• Excellent writing, editing, and communication skills.
• Ability to partner effectively with cross‑functional teams and SMEs.
• Experience working with controlled documentation and version control processes.
• Familiarity with electronic document systems (e.g., Veeva, Master Control) is a plus.
• Ability to work onsite 3–4 days per week.

Not Applicable

Full-time

Manufacturing

Pharmaceutical Manufacturing