- We act with integrity
- We serve each other
- We serve society
- We work for our future
At CAI, we believe in a relentless dedication to excellence, pushing boundaries and surpassing
expectations. From the beginning, we’ve challenged ourselves to do what others wouldn’t. Not just setting industry standards, but redefining them entirely. We are bold in our thinking and creative in our approach. 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. It’s a way of life. Because tomorrow demands to be at the forefront of today.
We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement. We’re not interested in how it used to be done. We’re obsessed with how it will be done. Key Responsibilities:
- 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).
Buone capacità relazionali e di lavoro in team.
Disponibilita' a trasferte italia ed estero se richieste
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 opportunità (l. 903/77)