About Us
We are a pioneering, family-owned pharmaceutical company dedicated to advancing the development and global commercialization of reproductive hormone therapies that support the lifelong health and well-being of both men and women.
Our products are widely used in gynaecology, fertility, obstetrics, and endocrinology.
With a presence in over 90 countries through a strong network of subsidiaries and distributors, we continue to grow sustainably. Today, we operate with approximately 1,500 employees, 22 subsidiaries, and 5 manufacturing sites.
Our continued success is built on attracting exceptional talent and fostering a collaborative, growth-focused environment.
Position:
Join our R&D Pharmaceutical Development team in Monaco and contribute to a portfolio of products for international markets. In this role, you will act as the key interface between CMOs/CROs/CDMOs and our CMC/Regulatory Affairs departments.
Key Responsibilities:
- Coordinate the scientific and technical activities of multiple development projects.
- Support the design and implementation of tools and processes for efficient project monitoring.
- Prepare, review, and manage project documentation, including protocols and reports, in both French and English.
- Analyze project requests, define development plans, and establish provisional timelines in collaboration with internal teams.
- Track project progress and ensure clear, proactive communication with all stakeholders.
Requirements:
- Bachelor’s or Master’s degree in Pharmaceutical Sciences, Biology, or a related health field.
- First experience in pharmaceutical development projects.
- Fluency in French and English, both written and spoken.
- Strong organizational skills, autonomy, and the ability to manage several tasks simultaneously.
- Excellent communication skills with a collaborative and team-oriented mindset.
Interested? Please apply and join us!
