QA Validation Specialist
2 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 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.QA Validation Specialist for 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-18808-Ljbffr
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Giuliano di Roma, 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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Roma, 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
3 giorni fa
Roma, Italia OSI Systems A tempo pienoBSP 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 2006. Innovation is the hallmark of BSP with investments in new technologies and production methods in a high...
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QA Validation Specialist
1 settimana fa
Roma, 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 2006. Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment...
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Pharma QA Validation Specialist — GMP
1 settimana fa
Roma, 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...
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Process & Computer System Validation Specialist (GCP)
2 settimane fa
Borca Di Cadore, Italia Altro A tempo pienoProcess & Computer System Validation Specialist (GCP)Direct message the job poster from Philogen S.p.A.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 Process & Computer System Validation Specialist (Gcp)RoleThe resource...
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Process & Computer System Validation Specialist (GCP)
2 settimane fa
San Pietro di Cadore, Italia K-ARRAY | Unique Audio Solutions A tempo pienoProcess & Computer System Validation Specialist (GCP) Direct message the job poster from Philogen S.p.A. 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 Process & Computer System Validation Specialist (Gcp) Role The...
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Process & Computer System Validation Specialist (GCP)
2 settimane fa
Borca Di Cadore, Italia Altro A tempo pienoProcess & Computer System Validation Specialist (GCP) Direct message the job poster from Philogen S.p.A.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 qualifiedProcess & Computer System Validation Specialist (Gcp)RoleThe resource...
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EQUIPMENT VALIDATION SPECIALIST
3 giorni fa
Roma, 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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Specialist in opleiding interne geneeskunde...
3 settimane fa
Roma, Italia Agap2 Italia A tempo pienoQA Validation Specialist Sede : Pomezia, Lazio( IT) Lingue: Italiano (obbligatorio), Inglese (preferibile) Modalità di lavoro: 3 giorni on-site, 2 giorni in smart working La risorsa sarà inserita nel team Quality Assurance con focus su attività di convalida e qualifiche in contesti produttivi farmaceutici sterili e di solidi orali. Il candidato ideale...
