Technical Writer
Medasource, Pleasant Prairie, WI, United States
Title: Technical Writer
Duration: 6-month contract
Location: Pleasant Prairie, WI
Key Responsibilities
• Review, assess, and improve existing:
o SOPs
o Work Instructions
o Training materials (OJT)
• Simplify and consolidate documentation to reduce redundancy and complexity
• Translate technical input from SMEs into clear, concise, and user-friendly procedures
• Partner with cross-functional teams (Ops, QA, Engineering) to gather requirements and
feedback
• Ensure all documentation aligns with GMP standards and internal quality systems
• Support improvements to onboarding and training by reducing documentation burden
• Work within electronic quality systems to manage and update controlled documents
Required Qualifications
• Experience as a Technical Writer in a GMP-regulated environment (pharma, biotech, medical
device, etc.)
• Background in Quality and/or Manufacturing Operations
• Hands-on experience writing and editing:
o SOPs
o Work Instructions
o GMP documentation
• Experience working in Veeva QMS
• Strong ability to translate complex technical concepts into clear, operationally usable
documentation
• Experience collaborating with cross-functional stakeholders
Preferred Qualifications
• Experience with MasterControl or similar document management systems
• Prior experience simplifying or optimizing large documentation systems
• Exposure to manufacturing floor operations and operator-facing documentation
- • Experience in startup or high-growth manufacturing environments