Medasource · 1 day ago
Technical Writer
Medasource is 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.
Health CareMedical
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
Qualification
Required
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
Ability to work onsite 3–4 days per week
Preferred
Familiarity with electronic document systems (e.g., Veeva, MasterControl) is a plus