Job Summary

• The role involves supporting the preparation of quality sections for clinical trial applications and marketing authorization files for biological products.
• Candidates will collaborate across global networks with drug substance development teams, analytical experts, and regulatory affairs specialists.
• The position offers an attractive remuneration package, 31 days of vacation, and opportunities to participate in transformation initiatives integrating artificial intelligence.

Matching Summary

Salary

Attractive remuneration on 12 months; Profit-sharing and bonus based on group results; Benefits include 31 days vacation, transport coverage up to 80%, and pension plans

Skills & Requirements

Key Requirements

• Master's degree (Bac+5) in pharmacy or engineering
• Fluent English proficiency required
• Prior knowledge of pharmaceutical quality standards

Work Rights