You will play a key role in the success of our development projects. Your responsibilities include:
Technical Expertise: Develop purification processes for active ingredients or intermediates ranging from the gram scale to several tens of kilograms (preparative liquid chromatography, batch, SFC, and SMB).
Project Management: Serve as the primary point of contact within your entity, ensure information relay to the Project Manager, and coordinate batch deliveries.
Outsourcing Management: Monitor externalized research projects by providing your expert perspective.
Scientific Rigor: Conduct bibliographic monitoring, write study reports, and participate in the management of the instrument fleet.
Compliance: Operate in a GMP (Good Manufacturing Practices) environment in strict compliance with HSE (Health, Safety, and Environment) rules.
Communication: Share the progress of your work with internal teams and management, ensuring clear and effective communication.
Your Profile
Education: PhD, Engineer, or Master 2 in organic chemistry, analytical chemistry, or process chemistry. Minimum 5 years of experience in preparative chromatography.
Hard Skills:
Experience in project management.
Experience in an environment compliant with Good Manufacturing Practices (GMP).
Knowledge and appetite for digital tools serving process development, such as DOE, AQBD, and Bayesian optimization.
Languages: Proficiency in English.
Soft Skills:
Autonomy, rigor, and organization.
Strong preference for operational field work.
Interpersonal skills and a critical mind, making you a recognized collaborator for your team spirit and proactive approach.
Don't forget to mention EuroPharmaJobs when applying.