CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field tested processes, and elite expertise developed over 30 years.
We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.

We serve each other
We serve society
From the beginning, we’ve challenged ourselves to do what others wouldn’t. We operate at the intersection of wisdom and technology and thrive when they come together with humanity. For us, operational readiness isn’t simply a goal. We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement. Scrittura, revisione e gestione dei Master Batch Record.




Supporto al progetto di transizione da Batch Record cartaceo a Electronic Batch Record (eBR).
Emissione, gestione e follow-up dei Change Control, coordinandosi con le diverse funzioni aziendali (Produzione, QA, Engineering, Validation, ecc.).
Supporto alle attività di compliance documentale secondo GMP.
~2–3 anni di esperienza in contesto farmaceutico GMP.
~ Esperienza nella gestione documentale di produzione e/o Change Control.
~ Buona conoscenza delle normative GMP.
~ Ottima conoscenza della lingua inglese (scritta e parlata).

The compensation package offered ranges from €34,000 to €45,000 gross per annum (Gross Annual Salary). The final salary within this range will be determined according to the candidate’s technical competencies and relevant professional experience.
La selezione rispetta il principio delle pari occasione (l. 34,000 - €45,000 a year
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📌 Quality Assurance Engineer (Batch Record and Change Control) (Milano)
🏢 Cai
📍 Milano