Position Details
About this role
This contract role involves creating technical documentation for immunohistochemistry testing systems in cancer diagnostics, ensuring regulatory compliance and supporting clinical workflows.
Key Responsibilities
- Develop user documentation
- Ensure compliance
- Establish SOPs
- Collaborate with scientists
- Support regulatory reviews
Technical Overview
Focus on clinical diagnostics, IHC testing, regulatory documentation, SOPs, and quality systems within a medical device and laboratory environment.
Ideal Candidate
The ideal candidate is a seasoned technical writer with at least 5 years of experience in diagnostics, laboratory medicine, or medical devices, capable of creating compliant user documentation and SOPs for clinical systems.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Less than 5 years experience, No experience in diagnostics or medical devices, Lack of technical writing background, Inability to work remotely
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