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stage 6 mois - affaires réglementaires

Gentilly, FR💼 Full-time🗓 2026-09-24 → 2026-09-25

Core

Support regulatory maintenance for a broad portfolio of general medicine products and assist in product launches.

Role type

Regulatory Affairs Intern

Builds

Regulatory submissions and product launch preparations

Domain

Biopharmaceuticals / General Medicine

Deliverable

client delivery

Required skills

Regulatory affairs knowledge, analytical thinking, synthesis skills

Preferred skills

None stated

Technologies

None stated

Responsibilities

Prepare and submit variation dossiers to ANSM and health authorities; Implement national and European AMM modifications (translations, packaging validation); Validate promotional documents against current references; Update databases; Collaborate with marketing, pharmacovigilance, and quality teams.

Seniority

Intern

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