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-LjbffrSenior IVD Regulatory Technical Writer in norcross at Unknown Company
This position is listed as full time and onsite.