QA Validation Specialist
4 giorni fa
GS Consulting, da oltre 10 anni fornisce consulenze per il settore Life Science in ambito QMS, Project Management, Validazioni, e CSV per aziende farmaceutiche.
A supporto della crescita aziendale, ricerchiamo un/una consulente con esperienza nell'azienda farmaceutica, con le seguenti mansioni:
redazione ed esecuzione dei documenti di qualifica del sistema (IQ/OQ/PQ) con strumentazione critica di qualifica;
Familiarità con la computer System Validation (CSV)
attività di Quality Assurance e Compliance in aderenza alle normative e linee guida di riferimento;
attività di Risk Management;
laurea triennale o magistrale in materie tecnico-scientifiche (Ingegneria Chimica, Chimica, Chimica Industriale, CTF, Farmacia, Biologia);
buona conoscenza della lingua Inglese sia scritta che parlata;
Roma
Orario di lavoro: full time
-
QA VALIDATION SPECIALIST
3 settimane fa
Latina, Provincia di Latina, Italia ManpowerGroup A tempo pienoManpower, 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...
-
QA VALIDATION SPECIALIST
2 settimane fa
Latina, Italia ManpowerGroup A tempo pienoManpower, 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...
-
QA VALIDATION SPECIALIST
2 settimane fa
Latina, Italia ManpowerGroup A tempo pienoManpower, 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...
-
Qa Equipment Validation Specialist — Gmp
1 settimana fa
LATINA, Italia Haupt Pharma Latina A tempo pienoA 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...
-
Pharma QA Validation Specialist — GMP
2 settimane fa
Latina, Italia OSI Systems A tempo pienoA pharmaceutical company in Lazio, Italy, is seeking a QA Validation Specialist for their Quality Assurance Validation Team. This role involves analyzing technical documentation, drafting Validation Protocols, and ensuring compliance with company protocols during validation processes. The ideal candidate should have a Master's degree in Chemistry or related...
-
QA Equipment Validation Specialist
1 settimana fa
Latina, Italia Haupt Pharma Latina A tempo pienoQA 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...
-
QA Equipment Validation Specialist
1 settimana fa
Latina, Italia Haupt Pharma Latina A tempo pienoQA 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...
-
Qa Equipment Validation Specialist
1 settimana fa
LATINA, Italia Haupt Pharma Latina A tempo pienoQA Equipment Validation Specialist for the site Borgo San Michele LT ItalyWould 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...
-
QA Equipment Validation Specialist — GMP
1 settimana fa
Latina, Italia Haupt Pharma Latina A tempo pienoA 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...
-
QA Equipment Validation Specialist — GMP
1 settimana fa
Latina, Italia Haupt Pharma Latina A tempo pienoA 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...