What are the responsibilities and job description for the Technical Writer position at Medasource?
Title: Technical Writer
Location: Lebanon, IN
Duration: 18 month contract (potential of extension)
Overview
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.
Key Responsibilities
- 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.
Qualifications
- 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, MasterControl) is a plus.
- Ability to work onsite 3–4 days per week.