pBSP Pharmaceuticals S.p.A is a CDMO with facilities for development and manufacturing across pre-clinical to clinical and commercial supply, including cytotoxic and high potent oncology drugs.
The role focuses on deviations investigations, validation protocol drafting, and audit support to maintain quality standards.
/ppThe candidate should possess an MA degree in Chemistry, English working knowledge, and a can-do attitude to work across departments and ensure compliance with SOPs and regulations.
/p #J-*****-Ljbffr
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.