*
Draft and compile regulatory submission dossiers for marketing authorization (MA) of pharmaceutical products.
*
Ensure scientific and regulatory compliance of all documents according to legal requirements and industry standards.
*
Collaborate with scientific and regulatory teams to gather necessary information.
*
Ensure that each dossier is complete, accurate, and tailored to the targeted markets.
*
Education: Bachelor's or Master's degree in Regulatory Affairs, Pharmacy, or Biology.
*
Experience: Relevant internship in the pharmaceutical sector or in regulatory dossier preparation.
*
Language Skills: Proficient in English (minimum B2), used on a daily basis.
*
Key Competencies: Detail-oriented, rigorous, with strong scientific and regulatory understanding.
*
Temporary contract with the possibility of permanent hire (CDI).
*
Competitive salary for a junior Regulatory Affairs Writer.
*
Benefits including meal vouchers, cafeteria plan, phone reimbursement, partial remote work (1 day/week), and group insurance (pension + life).
*
Professional development opportunities within a dynamic pharmaceutical environment.
*
Experience working with an experienced team and exposure to international regulatory practices.