Lavori attuali relativi a Qa Validation Specialist - LATINA - Bsp Pharmaceuticals S.P.A.

  • QA Validation Specialist

    5 mesi fa

    Latina, Italia BSP Pharmaceuticals A tempo pieno

    **Descrizione azienda**: 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...

  • Qa Specialist

    1 mese fa

    LATINA, Italia Bsp Pharmaceuticals A tempo pieno

    Descrizione azienda 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...

  • Qa Specialist

    1 mese fa

    LATINA, Italia Bsp Pharmaceuticals A tempo pieno

    Descrizione aziendaBSP 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...

  • QA Specialist

    4 settimane fa

    Latina, Italia BSP Pharmaceuticals A tempo pieno

    Descrizione azienda 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...

  • Qa Specialist

    4 settimane fa

    LATINA, Italia Bsp Pharmaceuticals A tempo pieno

    Descrizione aziendaBSP 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...

  • QA Specialist

    2 mesi fa

    Latina, Italia BSP Pharmaceuticals A tempo pieno

    **Descrizione azienda**: 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...

  • Quality Assurance Specialist

    3 settimane fa

    Latina, Lazio, Italia Bsp Pharmaceuticals A tempo pieno

    Join BSP Pharmaceuticals as a QA SpecialistBSP Pharmaceuticals is a leading Contract Development and Manufacturing Organization (CDMO) for anticancer drugs. We are currently seeking a highly skilled QA Specialist to join our Quality Assurance Team.The successful candidate will be responsible for ensuring the quality of our products by carrying out...

  • Validation and Compliance Specialist

    5 giorni fa

    Villa Latina, Lazio, Italia Stevanato Group A tempo pieno

    Job DescriptionWe are seeking a skilled Validation Specialist to join our Quality Validation team at Stevanato Group.The ideal candidate will have experience in validation activities in a multinational company, preferably in the pharmaceutical and medical devices industry.The successful candidate will be responsible for ensuring the approval and validation...

  • Quality Validation Specialist

    5 mesi fa

    Province of Latina, Italia Stevanato Group A tempo pieno

    Job Description We are looking for a Validation Specialist to join the Quality Validation team based in Cisterna di Latina (LT). Stevanato Group is an Italian but multinational manufacturing company. We develop and produce drug containment solutions in glass and plastics. The main production process is the the processing of the glass tube by...

  • QC Validation Specialist

    3 settimane fa

    Latina Scalo, Lazio, Italia Amaris Consulting A tempo pieno

    Job Opportunity: QC Validation AnalystWe are seeking a highly skilled QC Validation Analyst to join our team at Amaris Consulting, a leading provider of quality and laboratory services to the pharmaceutical industry.Key Responsibilities:Perform validation testing and analyze data to ensure the acceptability of analytical methods.Develop and implement...

  • QC Validation Specialist

    3 settimane fa

    Latina Scalo, Lazio, Italia Amaris Consulting A tempo pieno

    Job OpportunityAre you a detail-oriented professional with a passion for ensuring the accuracy and reliability of analytical methods? We are seeking a skilled QC Validation Analyst to join our team at Amaris Consulting.Key Responsibilities:Perform validation testing and analyze data to determine the acceptability of analytical methods.Collaborate with...

  • Quality Assurance Specialist

    2 mesi fa

    Villa Latina, Lazio, Italia Stevanato Group A tempo pieno

    Job Title: Quality Validation SpecialistJob Summary:We are seeking a highly skilled Quality Validation Specialist to join our Quality Validation team at Stevanato Group. As a Quality Validation Specialist, you will be responsible for ensuring the approval and validation of all production processes and supporting IT systems, as well as utilities, test...

  • Quality Assurance Specialist

    1 mese fa

    Villa Latina, Lazio, Italia Stevanato Group A tempo pieno

    Job Title: Quality Validation SpecialistJob Summary:We are seeking a highly skilled Quality Validation Specialist to join our Quality Validation team at Stevanato Group. As a Quality Validation Specialist, you will be responsible for ensuring the approval and validation of all production processes and supporting IT systems, as well as utilities, test...

  • Quality Assurance Specialist

    2 settimane fa

    Villa Latina, Lazio, Italia Stevanato Group A tempo pieno

    Job Title: Quality Assurance SpecialistWe are seeking a Quality Assurance Specialist to join our team at Stevanato Group. As a Quality Assurance Specialist, you will be responsible for ensuring the approval and validation of all production processes and supporting IT systems, as well as utilities, test methods, equipment, and cleaning processes, producing a...

  • QA Batch Record Review Specialist

    5 mesi fa

    Latina, Italia amaris A tempo pieno

    Job description QA Batch Record Review Specialist Cosa farai? Gestire processo di Batch Record Review a stretto contatto con il team di Quality Assurance. Lavorare su produzioni farmaceutiche sterili. Partecipare attivamente alle attività del progetto, dimostrando un approccio proattivo e iniziativa. **Requisiti**: Esperienza comprovata di 2-3 anni...

  • Quality Assurance Specialist

    1 giorno fa

    Villa Latina, Lazio, Italia Stevanato Group A tempo pieno

    Job Title: Quality Assurance SpecialistWe are seeking a highly skilled Quality Assurance Specialist to join our Quality Validation team based in Cisterna di Latina (LT).Stevanato Group is a multinational manufacturing company that develops and produces drug containment solutions in glass and plastics.The main production process involves the processing of...

  • Quality Assurance Specialist

    3 settimane fa

    Villa Latina, Lazio, Italia Stevanato Group A tempo pieno

    Job Title: Quality Validation SpecialistJob Summary:We are seeking a highly skilled Quality Validation Specialist to join our Quality Validation team at Stevanato Group. As a key member of our team, you will be responsible for ensuring the approval and validation of all production processes and supporting IT systems, as well as utilities, test methods,...

  • QA Specialist

    4 mesi fa

    Province of Latina, Italia Stevanato Group A tempo pieno

    Job Description Per il nostro Plant situato a Cisterna di Latina (LT) stiamo ricercando la figura di Quality Assurance Specialist. La persona, inserita all'interno del team di riferimento, avrà il compito di garantire la buona qualità del prodotto, interfacciandosi costantemente con produzione e allo stesso tempo anche con varie funzioni...

  • QA Compliance Specialist

    5 mesi fa

    Latina, Italia BSP Pharmaceuticals A tempo pieno

    **Descrizione azienda**: 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...

  • Pharmaceutical Plants Qualification Specialist

    5 giorni fa

    Latina, Lazio, Italia VTU A tempo pieno

    Pharmaceutical Plants Qualification SpecialistAbout the RoleAs a Pharmaceutical Plants Qualification Specialist, you will be responsible for the commissioning and qualification of pharmaceutical plants, as well as for their design. You will oversee the technical and organizational execution of the entire project.Your Key ResponsibilitiesProject management...

Qa Validation Specialist

3 mesi fa

LATINA, Italia Bsp Pharmaceuticals S.P.A. A tempo pieno

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 Organizations (CDMOs) for anticancer drugs.The fight against cancer is ours too.Position:We are currently looking for a QA Validation Specialist for our Quality Assurance Validation Team.Main Activities:Analysis of Technical Documentation: Ensure the analysis and evaluation of technical documentation related to manufacturing processes or cleaning and sanitization procedures that have to be submitted for validation.Defining Protocols: Drafting the Validation Protocols, by researching and acquiring data and information from other business functions.Validation: Ensure the correct validation of the processes and cleaning in compliance with company protocols and procedures through the execution of the operational activities.
Preparation of Validation Reports.Data Analysis: Ensure 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 organizationsKnowledge of GMPEnglish working knowledgeGreat can-do attitudeAt BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential.
We respect diversity, different backgrounds and experiences, and provide equal opportunity for all.We are BSP.
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