A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department. The role involves validating computerized systems to ensure compliance with GMP/GCP regulations, contributing to data integrity in clinical environments. Candidates should have a relevant degree, at least 2 years of experience in the pharmaceutical...
A leading biotech company in Italy is seeking a motivated Process & Computer System Validation Specialist to join their QA department. This role involves ensuring compliance with GCP regulations and maintaining computerized systems to safeguard data integrity. Candidates should have a technical degree, at least 2 years of experience in the pharmaceutical sector, and knowledge of regulatory...
Manpower, per azienda cliente del settore farmaceutico, sta ricercando un: QA Validation Specialist, che entrer a far parte del team di Quality Assurance Validation. Attivit principali: Analisi della documentazione tecnica Garantire l’analisi e la valutazione della documentazione tecnica relativa ai processi produttivi o alle procedure di pulizia e sanificazione da sottoporre a validazione....
Recordati is a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common...
A leading pharmaceutical contract manufacturer seeks a QA Equipment Validation Specialist in Latina, Italy. The role demands validation expertise ensuring compliance with industry standards, with a focus on sterile manufacturing processes. Candidates should have a degree in a scientific discipline and at least 3 years of experience in validation within the pharmaceutical sector. Strong GMP...
BSP Pharmaceuticals S.p. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxitc characteristics for the Pharmaceuticals Industry. BSP has been at the forefront in the fight agains cancer since ****. Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment plant. We are one of the most...
A prominent pharmaceutical manufacturer in Italy is seeking a QA Validation Specialist for their Quality Assurance Validation Team. This full-time position involves analysis of technical documentation, defining protocols, validation compliance, and data analysis. Candidates should hold an MA degree in CTF/Chemistry and have 1-2 years of relevant experience, with knowledge of GMP and working...
???? Posizione: QA Validation Specialist – Settore Farmaceutico ???? Sede: Anagni (FR) ???? Contratto: Tempo determinato Un'importante azienda farmaceutica è alla ricerca di una risorsa da inserire nel team di Qualification &, Validation, con possibilit di crescita professionale. ???? Attivit principali Supporto nella preparazione e revisione della documentazione tecnica (es. Validation Plan,...
Seleziona la frequenza (in giorni) di ricezione di un avviso: Tipo Lavoro: Dipendente Tipologia Contratto: Tempo indeterminato Località: Parma, IT Chi siamo Con sede a Parma, in Italia, Chiesi è un gruppo farmaceutico e sanitario internazionale focalizzato sulla Ricerca, con 90 anni di esperienza, che opera in 31 paesi con più di ***** dipendenti (Gruppo Chiesi). Per realizzare la sua missione di...
Una società di consulenza nel settore Farmaceutico cerca un Quality Assurance Specialist con almeno 5 anni di esperienza. Le responsabilità includono la gestione del sistema qualità e la preparazione di documentazione. È richiesta una laurea in discipline scientifiche e conoscenza delle GMP. L'ambiente di lavoro è dinamico e offre modalità ibride. Opportunità in diversi uffici in Lombardia e...
A leading biotech company in Italy is seeking a motivated Process & Computer System Validation Specialist to join their QA department. This role involves ensuring compliance with GCP regulations and maintaining computerized systems to safeguard data integrity. Candidates should have a technical degree, at least 2 years of experience in the pharmaceutical sector, and knowledge of regulatory...
A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department. The role involves validating computerized systems to ensure compliance with GMP/GCP regulations, contributing to data integrity in clinical environments. Candidates should have a relevant degree, at least 2 years of experience in the pharmaceutical...
QA Equipment Validation Specialist for the site Borgo San Michele LT Italy Would you like to make a valuable contribution to the health of patients And do something really meaningful on your own responsibility Then we look forward to hearing from you! Excellence beyond manufacturing - thats what we stand for as Aenova one of the worlds leading contract manufacturers and developers for the...
Recordati is a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common...
BSP Pharmaceuticals S.p. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxitc characteristics for the Pharmaceuticals Industry. BSP has been at the forefront in the fight agains cancer since ****. Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment plant. We are one of the most...
Manpower, per azienda cliente del settore farmaceutico, sta ricercando un: QA Validation Specialist, che entrer a far parte del team di Quality Assurance Validation. Attivit principali: Analisi della documentazione tecnica Garantire l’analisi e la valutazione della documentazione tecnica relativa ai processi produttivi o alle procedure di pulizia e sanificazione da sottoporre a validazione....
A leading biotech company in Italy is seeking a motivated Process & Computer System Validation Specialist to join their QA department. This role involves ensuring compliance with GCP regulations and maintaining computerized systems to safeguard data integrity. Candidates should have a technical degree, at least 2 years of experience in the pharmaceutical sector, and knowledge of regulatory...
BSP Pharmaceuticals S.p. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxitc characteristics for the Pharmaceuticals Industry. BSP has been at the forefront in the fight agains cancer since ****. Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment plant. We are one of the most...
A leading biotech company in Italy is seeking a motivated Process & Computer System Validation Specialist to join their QA department. This role involves ensuring compliance with GCP regulations and maintaining computerized systems to safeguard data integrity. Candidates should have a technical degree, at least 2 years of experience in the pharmaceutical sector, and knowledge of regulatory...
A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department. The role involves validating computerized systems to ensure compliance with GMP/GCP regulations, contributing to data integrity in clinical environments. Candidates should have a relevant degree, at least 2 years of experience in the pharmaceutical...