Global Submissions Regulatory Assistant II — Remote
Oklahoma City, Oklahoma County, Oklahoma, 73116, USA
Listed on 2026-10-02
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Science
Healthcare Compliance
Fortrea is seeking a Regulatory Affairs/QA document specialist to create, revise, compile, and approve specifications and submission documents for US, EU, Japan, and ROW authorities. You will collaborate with cross-functional teams to manage change controls, reviews, and labeling projects.
The role requires 1–2 years of relevant experience, strong MS Office skills, and knowledge of GMP/GxP guidelines. Office-based or remote work options are available with a focus on timely, compliant
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