QA Batch Record and Change Control
Pubblicato il 01-08-2026 - Cai in Milano
ph3CAI Overview /h3pCAI 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. /ph3Are You Ready? /h3pOur approach is simple because our Purpose informs everything we do: /pulliWe exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience. /li /ulpAt CAI, we are committed to living our Foundational Principles, both professionally and personally: /pulliWe act with integrity /liliWe serve each other /liliWe serve society /liliWe work for our future /li /ulpAt 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. /ph3Key Responsibilities /h3ulliScrittura, revisione e gestione dei Master Batch Record. /liliSupporto al progetto di transizione da Batch Record cartaceo a Electronic Batch Record (eBR). /liliEmissione, gestione e follow-up dei Change Control, coordinandosi con le diverse funzioni aziendali (Produzione, QA, Engineering, Validation, ecc.). /liliSupporto alle attività di compliance documentale secondo GMP. /lili2-3 anni di esperienza in contesto farmaceutico GMP. /liliEsperienza nella gestione documentale di produzione e/o Change Control. /liliBuona conoscenza delle normative GMP. /liliOttima conoscenza della lingua inglese (scritta e parlata). /liliBuone capacità relazionali e di lavoro in team. /li /ulpThe 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. /ppLa selezione rispetta il principio delle pari possibilità (l. 903/77) /p /p #J-18808-Ljbffr