Quality Assurance Engineer (Batch Record and Change Control)

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7cq5u7

Milano / ItalyEurope Life Sciences – South Europe /Full Time /HybridCAI Overview:Are You Ready?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.Our approach is simple because our Purpose informs everything we do:·

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We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.At CAI, we are committed to living our Foundational Principles, both professionally and personally:·

We act with integrity·

We serve each other·

We serve society·

We work for our futureAt CAI, we believe in a relentless dedication to excellence, pushing boundaries and surpassingexpectations. 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.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 possibilità (l. 903/77)34,000 - 45,000 a yearWe may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. xlwpduy Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7cq5u7