pBSP 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.
/ppThe 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.
/p #J-*****-Ljbffr
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