Regulatory Intern
On-site · Shanghai, Shanghai, China or Beijing, Beijing, China
Job Summary
Support regulatory documentation activities for Roche's China regulatory registration department: organize and compile registration materials (Modules 1-3), perform regulatory literature searches (NMPA, CDE, ICH), assist with electronic submissions (eCTD), stamping and archiving, and handle supplementary materials. Coordinate with production and quality teams, help archive project materials, and provide administrative support (meeting organization, minutes, PPTs). Strong Microsoft Office skills, English proficiency, proactive communication, and interest in the pharmaceutical industry are preferred. On-site roles in Shanghai or Beijing with at least 2 days per week on-site.
Required Qualifications
- Pharmacy or related majors; Pharmaceutical Engineering; Pharmacology/Drug Administration; Chemistry; Biology; currently enrolled bachelor-level or higher
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