Create, revise, and publish high-quality Instructions for Use (IFU) in alignment with current procedures, regulatory expectations, and market needs
Job Summary
Create, revise, and publish high-quality Instructions for Use (IFU) in alignment with current procedures, regulatory expectations, and market needs.
Collaborate cross-functionally with teams such as Product Development, Regulatory Affairs, Quality Assurance, Marketing, and Global Operations to gather information and validate technical accuracy.
Contribute to the continuous improvement of documentation standards, templates, and processes.
Matching Summary
Create, revise, and publish high-quality Instructions for Use (IFU) in alignment with current procedures, regulatory expectations, and market needs.
Skills & Requirements
Must-have
Instructions for Use (IFU) creation
Regulatory compliance (QSR, ISO)
Cross-functional collaboration
Style guide adherence
Content Management Systems (CMS/CCMS)
DITA/XML structured authoring
Nice-to-have
User-friendly content creation
Multilingual skills
Reusable content strategies
Cross-cultural communication
Attention to detail
Technical curiosity
Key Requirements
Bachelor’s or Master’s degree
2–3 years of technical writing experience
Life sciences, medical device, or IVD industry experience