Offerte di lavoro
>
Villa Latina

    Quality Validation Specialist - Province of Latina, Italia - Stevanato Group

    Stevanato Group
    Stevanato Group Province of Latina, Italia

    1 giorno fa

    Default job background
    Descrizione

    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 forming and the subsequent cleaning and sterilization of the container using highly automated machinery .

    The function of Validation team is to ensure the approval and validation of all production processes and supporting IT systems, as well as utilities, test methods, equipment and cleaning processes, producing a product that meets all applicable internal and regulatory requirements. The function is part of a corporate team, with multi-site responsibility .

    The figure will be involved in the following main activities:

    VALIDATION MANAGEMENT

    • Executes the qualification and validation activities in order to achieve the validation targets according with the level of services and timing defined into the approved plan, guaranteeing the compliance with applicable standards.

    • Supports the leader above in the definition of the qualification and validation activities, aimed at ensuring the compliance of the quality management system with applicable standards and requirements.

    • Provides timely and accurate all the validation documents, monitoring also thirds parts reports to be reviewed by the leader above for the final submission.

    • Participates alongside the Commercial Team to carry out new projects ensuring technical assistance and validation, as well as with R&D Team to define appropriate processes to guarantee the quality and reliability of the products.

    GUIDELINES AND PROCEDURES

    • Contributes to cascade accurate and up-to-date information related to regulations, customer requirements and other applicable standards to the team and to the other functions involved into the processes.

    • Support the validation practices definition, ensuring inclusion within the relevant quality management system.

    • Provides technical support to other functions involved in order to ensure the full application of the relevant quality management system for what concerns validations process.

    QUALITY AUDIT MANAGEMENT

    • Participates in the audit sessions as well as during the customers technical meetings in order to provide accurate and timely technical services and support for the relevant topic, executes corrective and preventive actions assigned
    working closely with the involved teams.

    REPORTING AND MONITORING

    • Elaborates appropriate reports in order to monitor KPIs related to validation and meet internal and external needs, highlighting timely deviations and critical issues and propose to the leader above actionable initiatives in order to achieve appropriately and effectively resolution.

    Qualifications

  • Scientific Master's Degree
  • +2 years' experience in Validation in a multinational company (preferably in a pharmaceutical and medical devices company)
  • Knowledge of the internal audit: process, features techniques
  • Knowledge of applicable regulatory, standards, global manufacturing practices;
  • Legal and standard requirements linked to the relevant applicable standard
  • IT Tool
  • Good English language proficiency
  • Availability to travel within the national territory is required.



  • Thermo Fisher Scientific Ferentino, Italia

    **Analysis of the technical documentation**: · Ensure, in agreement with the Supervisor, the analysis and evaluation of the documentation relating to the plants that must undergo qualification or requalification in order to acquire all the details necessary to issue the protocols ...


  • Thermo Fisher Scientific Ferentino, Italia

    Draft of Validation Protocols (cleaning, Process, Media Fill), by acquiring information from other departments to define their contents (e.g. process parameters, sampling plan) as well as collaborating with company functions to define actions to be carried out, as per company pro ...


  • MANPOWER ITALIA Ferentino, Italia PERMANENT

    Multinazionale operante nel settore chimico-farmaceutico · Manpower Group seleziona per Importante Multinazionale operante nel settore Chimico/Pharma la figura di EQUIPMENT VALIDATION SPECIALIST per la sede di Frosinone · Sei alla ricerca di una nuova sfida lavorativa nel settor ...


  • Adecco Italia Frosinone, Italia

    Ricerchiamo per conto di Azienda Cliente sita in provincia di Frosinone e operante in ambito chimico farmaceutico un Quality Assurance Specialist. La risorsa selezionata, nell'ambito del Gruppo di Quality Assurance e di concerto con il QA Manager e attraverso l'interazione con la ...


  • Thermo Fisher Scientific Ferentino, Italia

    When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your car ...


  • Thermo Fisher Scientific Ferentino, Italia

    When you're part of the team at Thermo Fisher Scientific, you'll do important and strategic work: you will help customers in finding cures for cancer and several diseases, also rare pathologies, working on new and innovative molecules for strategic therapies and most as promising ...


  • Thermo Fisher Scientific Ferentino, Italia

    When you join the team at Thermo Fisher Scientific, you'll be doing important and strategic work: helping customers to find cures for cancer and many other diseases, including rare pathologies, working on new and innovative molecules for strategic therapies and most promising and ...

  • UKSH Gesellschaft für IT Services mbH

    IT Specialist

    2 giorni fa


    UKSH Gesellschaft für IT Services mbH Germania, Italia

    IT Specialist (m/f/d) in the area of laboratory workstation in the field of clinical procedures · UKSH Gesellschaft für IT Services mbH, based in Lübeck, provides all IT services for the University Medical Center Schleswig-Holstein (UKSH) and thus supports cutting-edge medicine ...