Senior IVD Regulatory Technical Writer
Werfen
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. #J-18808-Ljbffr Werfen
Vacancy posted 3 days ago
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