31 lug - Parma
Altro
Experteer Italy is seeking a Global R&D; QA Specialist to lead validation of computerized systems in GXP environments, ensuring controlled state and compliance with regulatory expectations. You will collaborate across R&D; functions to align CSV activities with regulatory expectations and continuous improvement.
The role requires at least 5 years of CSV experience in the pharmaceutical industry, excellent knowledge of CFR 21 Part 11 and EU GMP Annex 11, and strong Data Integrity and risk
#J-*****-Ljbffr
06 ago - Torino
ITConsulting
06 ago - Reggio Emilia
K2 Partnering Solutions
06 ago - Torino
ITConsulting
06 ago - Cagliari
K2 Partnering Solutions