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
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
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
Productlife Group is seeking a Validation Specialist to plan, coordinate, and execute Computerized System and software validation activities for client projects in regulated environments across GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11.
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,
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
PQE Group cerca un Laboratory Equipment C&Q Expert da inserire a Roma per guidare qualifiche strumentali in un contesto laboratoristico GMP, supportando CSV e QA in riferimento a GxP e 21 CFR Part 11. Si richiede diploma/laurea
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
WYSER ricerca un/una Process Engineer per lo sviluppo, l’ottimizzazione e la validazione dei cicli di sterilizzazione destinati ai dispositivi medici. Responsabilità Sviluppare, ottimizzare e validare cicli di sterilizzazione (Steam & Low Temp) per dispositivi medici. Trasferire
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
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,
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,