QA Validation Specialist
1 settimana fa
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 2006.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 important Contract Development and Manufacturing Organization (CDMOs) for anticancer drugs.The fight against cancer is ours too.We are currently looking for a QA Validation Specialist for our Quality Assurance Validation Team.Main Activities:Analysis of technical documentationEnsure the analysis and evaluation of technical documentation related to manufacturing processes or cleaning and sanitization procedures that have to be submitted for validation.Defining ProtocolsDrafting the Validation Protocols, by researching and acquiring datas and informations from other business functions.ValidationEnsure the correct validation of the processes, cleaning in compliance with company protocols and procedures through the execution of the operational activities.Preparation of Validation Reports.Data AnalysisEnsure correct analysis of validation activities through data collection and analysis , in compliance with company protocols and procedures.Main Requirements:MA degree (CTF/Chemistry..);1/2 years of experience in similar roles in complex organizations;Knowledge of GMP;English working knowledge;Great can-do attitude.At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity , the different backgrounds and experiences and provide equal opportunity for all.We are BSP#J-18808-Ljbffr
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QA VALIDATION SPECIALIST
4 giorni 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...
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Qa Validation Specialist
4 giorni 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...
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QA VALIDATION SPECIALIST
3 giorni 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...
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QA VALIDATION SPECIALIST
3 giorni 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...
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QA Validation Specialist
1 settimana fa
Latina, Italia Altro A tempo pienoA leading pharmaceuticals company in Italy is seeking a QA Validation Specialist for its Quality Assurance Validation Team. The role involves analyzing technical documentation, defining validation protocols, ensuring compliance with cleaning processes, and preparing validation reports. Ideal candidates should possess an MA degree in a relevant field, have...
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Pharma Qa Validation Specialist — Gmp
4 giorni 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...
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Pharma QA Validation Specialist — GMP
5 giorni fa
Latina, Italia Altro 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...
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Pharma QA Validation Specialist — GMP
3 giorni 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...
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QA Equipment Validation Specialist
1 settimana fa
Latina, Italia Aenova Holding A tempo pienofor 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 - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for...
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Qa Validation Specialist
1 settimana fa
LATINA, Italia Manpower A tempo pienoManpower, per azienda cliente del settore farmaceutico, sta ricercando un:QA Validation Specialist, che entrerà a far parte del team di Quality Assurance Validation.Attività principali:Analisi della documentazione tecnicaGarantire l'analisi e la valutazione della documentazione tecnica relativa ai processi produttivi o alle procedure di pulizia e...
