The Regulatory Affairs Documentation/Records Specialist provides critical administrative and document support for worldwide product registration, import and tender activities, helping ensure products reach the patients who need them. This role primarily manages requests through email and request management systems and coordinates document authentication activities, including notarization, apostille and legalization. This position completes defined tasks accurately and on time, maintains clear records and status updates, and supports small projects under clear direction. Additional responsibilities may include product support activities such as data entry, document quality checks, record reconciliation and other administrative tasks.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED