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,
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
In this role you will lead and support Product Quality Complaint investigations for commercial and clinical products, working with manufacturing and regulatory teams worldwide. You ensure investigations are scientifically sound and well documented within the PQC
Process & Cleaning Validation Specialit I In this role you plan, execute, and document validation across equipment, processes, and computer systems to ensure product quality and regulatory compliance. You will collaborate with cross-functional teams to uphold
Thermo Fisher Scientific is seeking a Process & Cleaning Validation Specialist I to plan, execute, and document validation across equipment, processes, and computer systems to ensure product quality and regulatory compliance. You will collaborate with cross-functional
ALTEN supporta le strategie di sviluppo dei propri clienti nelle aree dell’innovazione, della R&D e dei sistemi informativi tecnologici. Attività principali Elaborazione di protocolli di cleaning (Cleaning Risk Assessment, Cleaning Validation Master Plan); Elaborazione di protocolli
Job Description 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
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. *
Ruolo: Computer System Validation - LIFE SCIENCE Si candidi qui sotto dopo aver letto tutti i dettagli e le informazioni di supporto relative a questa opportunità di lavoro. Luogo: Roma ALTEN supporta le strategie di sviluppo
About PhilogenPhilogen S.p.A. is a biotechnology company dedicated to developing targeted products for the imaging and treatment of life-threatening diseases, with a strategic focus on oncology. Our mission is to translate cutting-edge scientific innovation into effective
Ruolo: Computer System Validation - LIFE SCIENCELuogo: RomaALTEN supporta le strategie di sviluppo dei propri clienti nelle aree dell’innovazione, della R&D e dei sistemi informativi tecnologici.Nato più di 30 anni fa e presente in 30 Paesi,
We are looking for a Quality R&D Lead to join our Quality R&D team in Milan, supporting our Drug Delivery Systems (DDS) Business Unit.In this role, you will act as the Quality reference within product development
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,
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, and manage
In this Automation Engineer role at Novo Nordisk Anagni, you design, implement and optimise automation across the full lifecycle to boost production performance, compliance and patient delivery. You work within the Automation Engineering team to connect