Overview In PQE Group, la nostra divisione di Laboratory Excellence è in forte crescita grazie al mercato in continua evoluzione e alla crescente esigenza di qualità dei nostri servizi. Per questo motivo stiamo cercando figure di
ProductLife Group is seeking a Validation Specialist to lead CSV activities for client projects in alignment with GAMP 5, EU GMP Annex 11 and 21 CFR Part 11. The role centers on planning, documentation, and regulatory readiness
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dellindustria farmaceutica e dei Medical Devices? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle oltre
Specific activities and responsibilities Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11 requirements. Prepare, review,
Position Summary We are looking for a candidate that will join our team as a QC Laboratory Technician. The QC Laboratory Technician is responsible for assisting in administration of the quality functions at a site to
Validation Specialist (Data & Compliance) Location: Italy, Rome Workplace: Onsite Contract: Permanent Specific activities and responsibilities: Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5,
Electronical Process Engineer As a Process Engineer within BVI Medical’s Capital Equipment Operations team, you will be responsible for supporting the development, transfer, validation, and continuous improvement of manufacturing and testing processes for ophthalmic surgical consoles
Groupe ProductLife is seeking a Validation Specialist (Data & Compliance) to lead CSV activities on client projects in Rome, Italy. You will ensure compliance with GAMP 5, GMP, EU GMP Annex 11 and 21 CFR Part 11,
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dellindustria farmaceutica e dei Medical Devices? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle oltre
Job Description The QA Digital Compliance Manager is responsible for ensuring that all digital systems, records, instruments, processes and data handling within operations adhere to relevant regulatory, legal, best practices and industry standards. Key Responsibilities Monitoring
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Description Job Title: Environmental/ Energy Manager EEM Location: NAS Sigonella Scope: Ensures compliance with environmental, energy, and sustainability requirements. Responsibilities Implements the Environmental Management System (EMS). Prepares, submits, and maintains environmental permits, reports, and spill response
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Purpose As a Technology Transfer Engineer, you will lead operations for new technologies and platforms within the capital equipment division. Your responsibilities will include developing innovative solutions for manufacturing, testing, and validating cutting‑edge electro‑mechanical systems to
Job Details: Technology Transfer Engineer Full details of the job. Purpose As a Technology Transfer Engineer, you will lead operations for new technologies and platforms within the capital equipment division. Your responsibilities will include developing innovative
AGAP2 è un gruppo europeo di consulenza ingegneristica e operativa facente parte del Gruppo MoOngy. Presente in 14 paesi europei con oltre 7.500 dipendenti, abbiamo aperto, da quattro anni, la prima sede italiana a Milano e,
Il Gruppo Aeroporti di Roma, all’interno di Business Unit Aviation nell’unità organizzativa Asset Operations & Maintenance è alla ricerca di: AUTOMATION SYSTEMS ASSET OPERATION & MAINTENANCE ANALYST La risorsa, a diretto riporto del process owner, sarà
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dell’industria farmaceutica e dei Medical Device? In PQE Group, la nostra divisione di Laboratory Excellence è sempre in una fase di grande crescita
ALTEN è presente in Italia con sedi per progetti di validazione CSV nel Life Sciences. La posizione richiede esperienza nella redazione e gestione della documentazione di convalida, con attenzione alle normative EU Annex 11, FDA 21
Ruolo: Computer System Validation Consultant - LIFE SCIENCE Luogo: Roma ALTEN supporta le strategie di sviluppo dei propri clienti nelle aree dell’innovazione, della R e dei sistemi informativi tecnologici. Nato più di 30 anni fa e