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Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science. Proclinical is partnering exclusively with a clinical stage pharmaceutical company in the Paris region, to appoint a senior peptide development expert to lead CMC delivery for a long synthetic peptide programme moving rapidly towards first in human (Phase I). This is a high impact contract role for someone who can combine deep peptide technical expertise with hands on leadership across CDMO selection, tech transfer, scale up, formulation and CMC documentation.
Job Responsibility:
Lead process transfer, process development and optimisation for a synthetic peptide drug substance intended for non clinical and clinical use
Oversee scale up and ensure appropriate GMP alignment as the programme transitions into clinical supply
Define and drive formulation strategy and execution for injectable peptide formulations (with exposure to liquid and/or freeze dried (lyophilised) options)