I+D, farmacovigilancia y asuntos reglamentarios

I+D, Farmacovigilancia y Regulatory Affairs

Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

  • I+D, Farmacovigilancia y Regulatory Affairs

    Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

Título Ubicación Fecha Req ID Sort ascending
Restablecer
Senior Technical Leader, Protein Biologics Development, GRD CMC Parma, IT 10 sept 2026 7605
Senior Technical Leader, Analytical Method Development and Validation, GRD CMC Parma, IT 10 sept 2026 7606
Senior Technical Leader, GRD CMC
Senior Technical Leader, GRD CMC Parma, IT 10 sept 2026 7607
Parma, IT 10 sept 2026 7607
Senior Analytical Scientist - Bioassay CGT/ATMP
Senior Analytical Scientist - Bioassay CGT/ATMP Europe, remote, IT 26 ago 2026 7637
Europe, remote, IT 26 ago 2026 7637
Clinical Project Manager, Global Rare Diseases
Clinical Project Manager, Global Rare Diseases Europe, remote, IT 24 ago 2026 7642
Europe, remote, IT 24 ago 2026 7642
PV/RA Manager
PV/RA Manager Zaventem, BE 11 sept 2026 7643
Zaventem, BE 11 sept 2026 7643
Senior Process Scientist - LNP process development
Senior Process Scientist - LNP process development Europe, remote, IT 26 ago 2026 7645
Europe, remote, IT 26 ago 2026 7645
Clinical Partnership Manager
Clinical Partnership Manager Parma or Chiesi Affiliates in , IT 3 sept 2026 7659
Parma or Chiesi Affiliates in , IT 3 sept 2026 7659
Head of Clinical Data Innovation
Head of Clinical Data Innovation Remote, IT 2 sept 2026 7660
Remote, IT 2 sept 2026 7660