Lavori di CAI in Italia

Job summary · CAI is a professional services company that provides accelerated operational readiness and unparalleled performance through its rigorous approach, field-tested processes, and elite expertise. · ResponsibilitiesAt least 4 years of prior experience in QA, Validation, ...

We are 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 readi ...

Job Description: · The CQV Engineer develops documentation to support Commissioning Qualifications and Validation. · This includes protocol writing, field verification, and development of summary reports at client sites. · Key Skills include GMP-based knowledge, qualification pro ...

Position Description: · The Computer Systems Validation (CSV) Engineer develops and executes protocols and test scripts, identifies gaps, consults on plans for resolution. · writes GxP computer validation documentation · covers assessments, URS, FRS RTM summary reports · ...

Our company, CAI, is a professional services provider established in 1996. We have grown to nearly 750 people worldwide and specialize in operational readiness for Life Sciences and Mission Critical industries. · About Us · We act with integrity · We serve each other · We serve s ...

We are now seeking a CQV Engineer to join our growing operations in Italy. · ...

CAI Overview: Are You Ready? CAI is a professional services company established in 1996 with nearly · 800 people worldwide. · ...

We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. · ...

CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. · ...

A hands-on role responsible for the accurate and timely execution of financial reporting for the Italian legal entity. · ...

CQV Validation Engineer · Key Responsibilities: · Support Commissioning Qualification and Validation processes · Documentation and protocol writing for pharmaceutical projects · A leading company in Life Sciences seeks a CQV Engineer to ensure cGMP compliance. · ...

Estamos buscando un CQV Engineer para unirnos al nuestro equipo Operation en crecimiento en Italia. El CQV Engineer se encarga de la documentación relativa a Comisionado, Calificaciones y Validación. · Elevada atención a los detalles. · Capacidad de multitasking y de tomar la ini ...

Stiamo cercando un CQV Engineer per unirsi al nostro team Operation in crescita in Italia. · Elevata attenzione ai dettagliCapacità di multitasking e di prendere iniziativa per portare a termine i compiti assegnati con precisione, · suo secondo quanto stabilito.Laurea triennale o ...

Stiamo cercando un CQV Engineer per unirsi al nostro team Operation in crescita in Italia. · ...

We are seeking a Process Engineer to join our team at CAI. · Pharma GMPs main regulations knowledge · Cleaning Validation Experience · ...

The Computer Systems Validation (CSV) Engineer will develop and execute protocols and test scripts, identify gaps, and consult on and direct plans for resolution.This person is responsible for writing GxP computer validation and 21 CFR Part 11 related documentation such as assess ...

This position uses policies and procedures to validate/qualify computer systems, · prioritizes in a compliant validation process for quality information technology · and automation systems which require formal validation documentation under appropriate regulatory requirements. · ...

Se busca un CQV Engineer para unirte al equipo de operaciones en crecimiento en Italia. Serás responsable de documentación relativa a Commissioning, Qualifiche y Validación. · ...

We are now seeking a Validation Engineer to join our growing operations in Italy.The role of a Validation Engineer in CAI is to support documentation for the Commissioning, Qualification, · & Validation of pharmaceutical facilities, utilities, · & equipment. · ...

Job summary · We provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach. · ...