Descrizione dell'offerta
Experteer Italy seeks a seasoned leader to define and govern automation standards for PAS platforms across Biotherapeutic and Synthetic sites. You will drive library governance, roadmaps, and cross-site alignment with global teams to ensure compliant, reliable automation environments.
The role requires deep PLC/SCADA/DCS knowledge, ISA S95/S88, and experience with cGMP, 21 CFR Part 11, and EU GMP Annex 11. English fluency is essential; travel up to 25% is anticipated.
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Candidatura e Ritorno (in fondo)
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