Non-Clinical Formulation Lead
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Make your mark for patients
We are looking for a Non-Clinical Formulation Development Lead who is collaborative, curious, and solution-focused to join our Developability and In Vivo Performance team, based in Braine-l’Alleud, Belgium.
About the role
You will shape formulation strategies for small molecules, peptides, and other synthetic medicines from discovery through non-clinical development. You will provide scientific direction for formulation screening and regulated studies, connect scientific teams, and help orient future clinical formulations. Using your expertise, you will translate complex data into clear development decisions and regulatory documentation, while fostering innovation and exploring new ways of working that improve scientific quality, agility, and impact.
Who you’ll work with
You will be working in a team that brings together formulation, biopharmaceutics, drug metabolism, laboratory operations, and drug product development expertise. You will collaborate with internal and external partners, facilitate communication across research and development functions, and support an integrated development strategy.
What you’ll do
You will shape formulation strategies from discovery through non-clinical development.You will coordinate the drug product project team during preclinical development.
You will design experiments, interpret data, and recommend clear scientific actions.
You will oversee formulations supporting regulated toxicology, cardiovascular, and telemetry studies.
You will manage scientific activities with internal teams and external partners.
You will champion innovation, challenge established approaches constructively and introduce new ways of working to increase efficiency and scientific impact.
You will author regulatory documents and connect research and development functions.
Interested? For this role we’re looking for the following education, experience and skills
Master’s degree in a relevant scientific discipline.Ideally, 5 years’ pharmaceutical development, manufacturing, or biopharmaceutical experience.
Formulation expertise across drug substance, drug product, analytical, or biopharmaceutical development.
Knowledge of regulated quality practices and pharmaceutical regulatory requirements.
Experience preparing clear scientific and regulatory documentation.
Strong interest in innovation, continuous improvement, and experimenting with new ways of working to solve scientific and operational challenges.
Ability to adapt and thrive in an evolving organization, remaining agile and effective as priorities, structures, and ways of working change.
Confident English communication, collaborative working, project planning, and risk management skills.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you
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