Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.
VALIDATION SPECIALIST JUNIOR Il Validation Specialist sarà di supporto al team di Validazione interno di stabilimento per la pianificazione, esecuzione e gestione delle attività di validazione per garantire che gli impianti e i sistemi siano conformi
A prestigious company operating in the Pharma / Life Sciences sector has entrusted us with the search for a: PART-TIME CONTRACT DURATION: 18–24 months START DATE: May 2026 Do you have experience managing complex changes in highly
Process & Computer System Validation Specialist (GCP) Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti‑tumor therapies, is looking for a highly motivated and qualified
Job Description Summary The Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, focusing on developing and deploying global standards that improve the reliability, availability, and performance of Aero Alliance’s manufacturing equipment
Job Description Summary Job Description Summary Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, focusing on developing and deploying global standards to improve the reliability, availability, and performance of Aero Alliance’s
Job Description Summary The Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, the primary focus area will be developing and deploying global standards that improve the reliability, availability, and performance of
Job Description Summary The Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, the primary focus area will be developing and deploying global standards that improve the reliability, availability, and performance of
Job Description Summary The Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, focusing on developing and deploying global standards that improve the reliability, availability, and performance of Aero Alliance’s manufacturing equipment
Job Description Summary The Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, the primary focus area will be developing and deploying global standards that improve the reliability, availability, and performance of
Orienta Spa – Società Benefit – filiale di San Bonifacio ricerca un/una Automation Engineer / Computer System Validation Specialist per realtà di consulenza operante in ambito regolato (farmaceutico/biotech). ATTIVITÀ / MANSIONI ·Gestione fornitori e system integrator
Orienta Spa – Società Benefit – filiale di San Bonifacio ricerca un/una Automation Engineer / Computer System Validation Specialist per realtà di consulenza operante in ambito regolato (farmaceutico/biotech). ATTIVITÀ / MANSIONI ·Gestione fornitori e system integrator
Orienta Spa – Società Benefit – filiale di San Bonifacio ricerca un/una Automation Engineer / Computer System Validation Specialist per realtà di consulenza operante in ambito regolato (farmaceutico/biotech). Gestione fornitori e system integrator per nuovi progetti
Orienta Spa – Società Benefit – filiale di San Bonifacio ricerca un/una Automation Engineer / Computer System Validation Specialist per realtà di consulenza operante in ambito regolato (farmaceutico/biotech). ATTIVITÀ / MANSIONI ·Gestione fornitori e system integrator
Orienta Spa – Società Benefit – filiale di San Bonifacio ricerca un/una Automation Engineer / Computer System Validation Specialist per realtà di consulenza operante in ambito regolato (farmaceutico/biotech). Si candidi in fretta: consulti la descrizione completa
Overview Orienta Spa, Società Benefit filiale di Verona seleziona COMPUTER SYSTEM VALIDATION & DATA INTEGRITY CONSULTANT – GMP per realtà operante nella consulenza con sede a Verona. La risorsa verrà inserita in progetti presso aziende farmaceutiche
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
Milano / ItalyEurope Life Sciences – South Europe /Full Time /HybridPosition Description: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.
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