Careers
Making a Difference in European
Healthcare
At AzurBio Pharma, our mission is to ensure that cutting-edge therapies reach those in need as quickly and efficiently as possible. We’re seeking talented and passionate individuals to join our team as we strive to make a lasting impact on healthcare.
Join our Team
If you’re excited about shaping the future of the pharmaceutical industry in Europe, we invite you to explore our current job opportunities and discover how you can contribute to our mission.
Current job openings
Director, Regulatory Affairs - Europe
Full time
We are seeking a motivated and rigorous Regulatory Affairs Director (M/F) to join our European Operating Unit.
The Director, Regulatory Affairs – Europe will provide expert regulatory insight and operational support across client projects, ensuring high-quality service delivery in their area of expertise.
This role involves maintaining strong client relationships, guiding consulting teams, resolving complex regulatory challenges, and contributing to commercial proposals.
Associate Director, Regulatory Affairs - Europe
Full time
We are looking for a motivated and rigorous Regulatory Affairs Associate Director (M/F) to join our European Operating Unit.
The Associate Director, Regulatory Affairs – Europe will provide expert regulatory insight and operational support across client projects, ensuring high-quality service delivery in their area of expertise.
This role involves maintaining strong client relationships, guiding consulting teams, resolving complex regulatory challenges, and contributing to commercial proposals.
Project Management Director
Full time
We are seeking a motivated and detail-oriented Project Management Director (M/F) to join our European Operating Unit.
You will ensure effective coordination and operational excellence across clients’ projects from development and registration to launch and maintenance.
Working closely with the leadership and consultant teams, you will help plan and deliver projects on time, within scope, and on budget, while supporting the team in navigating scientific, regulatory and operational challenges.
Quality Consultant – Exploitant
Full time
We are seeking a motivated Quality Consultant– Exploitant (M/F) to join our team and ensure technical excellence in quality management, supporting compliance and operational excellence.
You will ensure compliance, quality oversight, and operational excellence across our Exploitant activities in France. You will also support product launches and maintain constructive interactions with health authorities.
Working closely with internal teams and clients, you will provide expert guidance on quality matters, drive continuous improvement, and ensure adherence to the highest compliance standards.
Internship - Regulatory affairs, quality & pharmacovigilance
Internship
We are looking for a motivated and rigorous intern to support the operations team, regulatory affairs, quality & pharmacovigilance.
Under the supervision of a manager or the Head Pharmacist, you will play an active role in the life of our pharmaceutical "Exploitant" activities, supporting our customers and our team in a variety of areas.
Are you a pharmacy student (in your fifth year or above) looking for an internship with a wide range of practical tasks, at the heart of regulatory and drug quality issues? Join us and help advance access to innovative treatments in Europe.