Qa Validation Specialist
3 giorni fa
BSP Pharmaceuticals S.p. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxic characteristics for the Pharmaceuticals Industry.BSP has been at the forefront in the fight against 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 important Contract Development and Manufacturing Organization (CDMOs) for anticancer drugs.The fight against cancer is ours too.QA Validation Specialistfor our Quality Assurance Validation Team.Main ActivitiesAnalysis 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 data and information 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 RequirementsMA degree (CTF/Chemistry..)1/2 years of experience in similar roles in complex organizationsKnowledge of GMPEnglish working knowledgeAt 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.Seniority levelMid-Senior levelEmployment typeFull-timeJob functionQuality AssurancePharmaceutical ManufacturingGet notified about new Quality Assurance Specialist jobs in Latina, Latium, Italy.#J-*****-Ljbffr
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Qa Validation Specialist
1 settimana fa
Lazio, Italia Agap2 Italia A tempo pienoQA Validation Specialist Sede: Pomezia, Lazio( IT)Esperienza richiesta: 5–10 anniLingue: Italiano (obbligatorio), Inglese (preferibile)Modalità di lavoro: 3 giorni on-site, 2 giorni in smart workingSettore: Farmaceutico – impianti sterili e solidi oraliDescrizione del ruoloLa risorsa sarà inserita nel team Quality Assurance con focus su attività di...
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Lazio, Italia Osi Systems A tempo pienoA leading pharmaceutical company in Italy is looking for a QA Validation Specialist for its Quality Assurance Validation Team.The role involves analysis of technical documentation, drafting validation protocols, ensuring validation compliance, conducting data analysis, and preparing reports.Candidates should have an MA degree in a relevant field, 1-2 years...
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Qa Validation Specialist
7 giorni fa
Lazio, Italia Altro A tempo pienoBSP 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...
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Qa Validation Specialist
7 giorni fa
Lazio, 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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Pharma Qa Validation Specialist — Gmp
1 settimana fa
Lazio, Italia Crazy Pizza A tempo pienoA leading pharmaceutical company in Italy is seeking a QA Validation Specialist to join their Quality Assurance Validation Team.This mid-senior level role involves analyzing technical documentation, drafting validation protocols, and ensuring compliance with GMP standards.The ideal candidate holds a MA degree in CTF or Chemistry and has 1-2 years of relevant...
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Qa Validation Specialist
1 settimana fa
Lazio, Italia Crazy Pizza A tempo pienoBSP Pharmaceuticals S.p. A focuses on the development and manufacturing of anticancer drugs with high potency and cytotoxic characteristics for the pharmaceutical industry.BSP has been at the forefront in the fight against cancer since ****.Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment...
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Process & Computer System Validation Specialist
3 giorni fa
Lazio, Italia Altro A tempo pienoPhilogen 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 qualifiedProcess & Computer System Validation Specialist (Gcp)RoleThe resource will join theQA departmentand will be responsible for the validation and maintenance of the company's...
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Equipment Validation Specialist
1 giorno fa
Lazio, Italia Ayes - Management & Technology Consulting A tempo pienoFai la differenza con AYES: unisciti come EQUIPMENT VALIDATION SPECIALIST!AYES, multinazionale di consulenza ingegneristica e tecnologica, in vista dell'espansione delle proprie attività in Italia, è alla ricerca di un EQUIPMENT VALIDATION SPECIALIST da inserire su progetti strutturati nel settore farmaceutico.AYES opera a livello globale, offrendo...
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Equipment Validation Specialist
1 giorno fa
Lazio, Italia Ayes - Management & Technology Consulting A tempo pienoFai la differenza con AYES: unisciti come EQUIPMENT VALIDATION SPECIALIST!AYES, multinazionale di consulenza ingegneristica e tecnologica, in vista dell'espansione delle proprie attività in Italia, è alla ricerca di unEQUIPMENT VALIDATION SPECIALISTdainserire su progetti strutturati nel settore farmaceutico.AYES opera a livello globale, offrendo soluzioni...
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Qa Specialist
1 giorno fa
Lazio, Italia Adecco A tempo pienoAdecco Lifescience, per importante azienda leader nel settore farmaceutico, è alla ricerca di una figura di QA Specialist, il quale avrà il compito di garantire che tutte le attività aziendali siano conformi agli standard normativi (GMP, GDP, ISO) e alle politiche interne, supportando i processi di audit, gestione dei rischi e miglioramento...
