BSP Pharmaceuticals S.p.A invites a skilled QA professional to join our CDMO operations in Italy. You will review batch records, support investigations, and help keep GMP documentation up to date across QA and manufacturing areas.
The role emphasizes compliance, change control, and safety, requiring a strong attention to detail and the ability to draft clear reports in English. Competitive salary and career growth offered in a multinational setting.
📌 GMP QA (Latina)
🏢 BSP Pharmaceuticals
📍 Latina
Candidati a questo annuncio
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.