Medasource
Technical Writer Location: Lebanon, IN
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.
Excellent writing, editing, and communication skills.
Familiarity with electronic document systems (e.g., Ability to work onsite 3–4 days per week.