Senior IVD Regulatory Technical Writer
Listed on 2026-10-01
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Research/Development
Werfen seeks a Sr. R&D Technical Writer to prepare technical documentation for IVDR and FDA submissions. You will work with Regulatory Affairs, Quality Control, Clinical Operations and Project Management to ensure compliant, precise documentation of products.
You will draft plans, protocols and reports, mentor junior staff, and contribute to continuous improvement of documentation practices. On-site work in Norcross, GA is required, with potential to influence global regulatory submissions.
The following opportunity is for a Senior IVD Regulatory Technical Writer with Werfen.
We are seeking a motivated Senior IVD Regulatory Technical Writer to join Werfen in Norcross, GA, United States.
Consider building your career as a Senior IVD Regulatory Technical Writer at Werfen.
The Senior IVD Regulatory Technical Writer position in the Bio & Pharmacology & Health, Engineering field is open for applications.
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