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Niveau van het gemiddelde loon tijdens de laatste 12 maanden: "IT specialist in "

Valuta: EUR USD Jaar: 2020
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Indeling van de "IT specialist" vacatures in de regionen

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Volgens het diagraam zijn er in het grootste aantal vakatures van de beroep IT specialist in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Top van de gelijkaardige vacatures volgens niveau van het loon in

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Volgens het diagraam zijn er in het grootste aantal vakatures van de beroep IT specialist in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Aanbevolen vacatures

Specialist, Incoming Material Bioprocess & Single Use Systems
GSK, Wavre, Walloon Region, be
The SPU Incoming Material department is managing life cycle of Incoming Material (IM) used by all Belgian Manufacturing Production Unit’s (MPU)The team is focusing on Single Use Systems (SUS), Filters & Purification Items (gel, UF membrane, …) such as bag for sterile bulk distribution in New IPV & New HAV facilities.Managing lifecycle of SUS & Filters means being part of different steps: definition, qualification, implementation, deviation support and change notification management.As IM and SUS Bioprocess Specialist, you are in close connection with all Belgian MPU’s to support them in all steps described above. Gemba’s & workshop on the shop floor are part of the day to day job.You will also be involved in audit (internal & external) to bring your expertise to answer any question from auditors linked to SUS & Filters.Your responsibilities:Individually or as part of a project team, you will be responsible for solution design & qualification to be implemented in primary & secondary process.You will be responsible for the execution, coordination and follow-up of solution designs and technical matters related to Single Use Systems to ensure production, transformation, commissioning and qualification of the solution meets agreed cost, timing, technology and quality standards in line with the Engineering standards.In case of deviation, you will be responsible to investigate potential root cause (within GSK & at the supplier), write appropriate justification in the deviation.You will act as SME for dedicated Single Use System Key activities include:Define functional, technical and quality requirements.Ensure preparation and update of the project qualification and coordinate qualification activities of the systems.Ensure coordination of a multifunction team to enable the creation of single use articles following the internal procedures.Ensure correct systems implementation through training, SOP writing and assistance to the production team.Ensure investigation follow up in case of deviationEnsure definition & implementation of transversal CAPAWhy you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:University degree in Engineering (or equivalent by experience)3 to 5 years experience in GMP environmentFluent in French and English (spoken and written)Preferred Qualifications:If you have the following characteristics it would be a plus:Basic knowledge in Plastics & Plastics Processing (injection, moulding, …)Knowledge of qualification/validation principles (V cycle, URS, IOQ, …)Knowledge of pharmaceutical, aseptic and biotech processesFamiliar with Risk Analysis (FMEA) & Quality by design approachesAutonomous, Rigorous, Structured, Systematic, Good analytical skillsAbility to lead and impact cross-functional team members without hierarchical authorityQuality orientedExperience as investigator/ supplier auditor is an advantageExperience as trainer / setting up training packages is an advantage*Li-GSK
SPECIALIST INDUSTRIAL IT UNIFY PROGRAM / M,F,X
ArcelorMittal, Liuege, Wallonia
Are you fascinated by IT and software architecture? Would you like to work in a high-tech IT environment? Then maybe you are the person we are looking for! Read onWhat does the job involve?As a specialist in industrial IT, you will take part in a large transformation program aiming at unifying the production lines follow-up solutions and logistic solutions between ArcelorMittal Belgium plants. You will be in charge of various projects/tasks in the program like development, analysis, business support and project management. Multiple IT & business teams from Liège and Ghent will be you direct contacts.You will grow in an international company where you will have the opportunity to take on different roles or projects in both Liège and Ghent.Are you the right candidate?You have knowledge of architectural designs (3 tiers, DDD, microservices,…) and C# language.You have the ability to challenge customer ideas and find consensus.You are open to new knowledge and ideas.You are comfortable with software design concepts.You are sociable and able to easily fit in an already existing team.You are open to travel to Liège and Ghent (main location: Liège).You are fluent in French and English, fluency in Dutch is a plus.This gives you great bonus points:Proven records / experience in large IT projects (both as analyst and as developer)Experience with IT solutions for heavy industry processes is a plusExperience with Angular is a plusDiversity and inclusion make us even stronger!ArcelorMittal Belgium is all about equal opportunities and values diversity. We select candidates solely on the basis of their competences. Your age, gender, ethnic origin, orientation, religion, disability, nationality, … do not influence your chance to help build sustainable circular steel solutions for the future.
Senior Specialist - Automation Engineer
GSK, Rixensart, Wallonia
Job Purpose:This position can be based in Rixensart - Belgium OR Siena - Italy.As the Senior Specialist – Automation Engineer, you are expected to provide robotics engineering support with the primary objective of developing automated processes and analytical methods relying on the usage of robotic technologies.Your Responsibilities:You will be responsible for driving the transformation of Drug Substance development towards task automation and robotic control.You will establish new automation applications for our existing platforms (e.g. TECAN, Hamilton and AmbR).You will drive the system integration of separated pieces of equipment in a controlling unit relying on PAT (Process Analytical Technology)/sensors.You will collaborate with Scientists to translate existing manual procedures into automated workflows integrating new assets on automation platforms, ensuring optimal efficiency & performance.You will develop performance and qualification procedures for the maintenance of automation platforms.You will define and follow continuous improvement for the lifecycle of automated systems, including system troubleshooting and upgrade.You will develop introductory equipment training packages and train equipment users on key concepts associated with the robotic platforms to support best-practice and mitigate avoidable run failures, ensuring optimal routine operation.You will establish and maintain strong relationships with vendor application specialists.You will stay up to date regarding new developments in the field of laboratory automation and inhouse new standards.You will help develop best-practice and facilitate knowledge sharing between automation SME’s at GSK within Technical R&D as well as equivalent based in other functions outside of Technical R&D (QC, MSAT, Clinical Laboratory Studies, Preclinical, Pharma, etc.)*LI-GSKWhy you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Master’s degree in Electro-Mechanic Engineering, Process Automation, Robotics or related field with 5+ years of experience.Min 5 years’ experience in lab instrument support or in process automation preferably in the Biopharma industry is required.Expertise in Commissioning and Validation of automation systems.Understanding of device networking and communications protocols.Extensive experience writing protocols in Evoware & Venus software.Experience in installing & servicing large integrated systems.Experience with PAT and automated control units.Influencing skills & bringing people on board is essential for you to be able to drive the transformation of Drug Substance development towards automated processes.Proficiency in English is a MUST & French/ Italian are a Plus.Preferred Qualifications:If you have the following characteristics it would be a plus:Must have the ability to work in a multidisciplinary environment and communicate effectively.Optimistic mindset.Customer-oriented.Easy social networking/ interfacing.Have the skills & capacity to train others and be able to translate complex material into “simple” content for day-to-day use by the Scientists.The ability to effectively work and perform within a team of related platform staff is essential.Must have the ability to work with cross-functional teams and communicate effectively.Have the capacity to coordinate a small group to implement studies from development projects.
Specialist, QA
GSK, Wavre, Walloon Region, be
The purpose of the role is to assure and maintain the organization of the activities linked to the quality oversight of the manufacturing activities in the production building ofShingrixbulkproduction. By the quality oversight of the manufacturing process and the use of quality systems in place, ensure the quality of the product and the supply of the bulk product in a timely mannerYour responsibilities: Represent Quality assurance in the decision linkedto themanufacturing activitiesParticipate the improvement of the quality systems in the production building to assure compliance of consistency campaign and the commercial productionEnsure and organize the implementation of quality oversight activities linked to the documentation review (Check-lists, batch-records..) Identify, Develop and Implement improvements to the quality oversight processesTraining and coachingmanufacturing onefficient deviation management and risks identification, including facilitating and/or contributing to risk identification workshops or root cause analysis for deviations.*LI-GSKWhy you?Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:University degree:master degree in Sciences/Engineering e.g. Pharmacist / Master in Sciences / Bio Engineer pharmaceuticalMinimum 5 years in the Pharmaceutical/Biotech industry with significant experience of GMPFrench fluent and professional writing and speaking in English are a must. Preferred knowledge of vaccines and/or immunology process and products (manufacturing).Preferred Qualifications: If you have the following characteristics it would be a plus:Minimum of 1-2 years of experience in manufacturing and/or QA within the pharmaceutical industry.Good knowledge of cGMPAutonomyGood interpersonal and communication skillsDemonstrated ability of stakeholder managementDemonstrated experience in influencing improvement activity to ensure implementation of appropriate actionsKnowledge of primary processes is an asset
Sr. Logistics Specialist
Ascend Performance Materials, Ottignies-Louvain-la-Neuve, Walloon Region, be
Position SummaryThe Logistics Specialist is responsible for optimizing transportation and logistics costs and service levels by continually improving the processes and networks by which the business utilizes trucking, rail, air, and ocean transportation modes. He/she is fully engaged in responsible movement of Ascend materials to and within the European region, Middle East, Africa and India. The Logistics Specialist is also responsible to work with the global procurement team and source, negotiate & manage local logistic contracts and services as required.Logistics Specialist EMEAI Duties and ResponsibilitiesSupport Day to Day activities using Logistics expertise to allow flows to run seamlesslyDrive efficiency projects to reduce transportation/logistics costs across the board. Taking transport modes, payloads and lead times into account.Set costs targets/benchmarks and execute accordingly and drive Cost-awareness throughout the Supply Chain Team.Assists the EMEAI team with establishing, monitoring and making adjustments to the logistics budget.Drive improved automation through the CSR/SIOP/Logistics process.Responsible for all transportation activities in accordance with organization’s policy and procedure and in line with local, country and international law.Responsible for operations of 3rd Party warehouses. Monitor 3PL warehouse in/out/storage activities and costs associated with it.Manage 3PL/4PL logistics and transportation activities, develop and maintain performance KPI’s, review logistics performance against KPI, benchmarks and service agreements and serve as liaison between 3PL, 4PL and Ascend. Responsible for logistics and transportation related dispute resolution activities & insurance claims/risk management as delegated.Stay informed of logistics technology advances and recommend applying appropriate technology in order to improve logistics processes. Related topics are: TMS, automated freight bill control, 4PL control tower.Taking responsibility for the management of the Logistics Cost process for the region and ensure fully Freight-costing setup in SAP.Maintain the relevant cost KPI’s together with the Logistic Team Leaders, Contract Manager and Customer Fulfilment Manager.Contact vendors with regards to invoice related issues.Help analyze top down plans and projects on cost impactStay informed of latest developments in packaging materials and packaging requirements in order to comply with product quality, safety regulations and customers’ needs. Recommend new packaging materials and packing processes.Develop an understanding of customers' needs on logistics and transportation and take actions to ensure that such needs are met.Receive, investigate, verify and resolve customer complaints on logistics and transportations.Ensures systems for meeting export, import, and all other logistics compliance requirements.Provide logistics support activities, such as estimating cost related to delivery and storage. Answer questions on cost, contract requirements and chronic performance issues.Build relationship with logistic services providers and carriers by means of periodical visits.Perform periodical audits and quality checks of logistic service providers and carriers.Manage SAP Purchase and Blanket Orders accordingly.Be fully familiar with ESSH and ethical procedures (Code of Conduct)Continuous attention to improve safety, quality, service and cost performancePermanent attention to deliver the best-in-class business service by using the existing network logistics providersAct as a safety leaderThis role will report directly to the Supply Chain ManagerDirect Reports: NoneRequired ExperienceMinimum 4 years working experience in multinational companies in logistics/supply chain functions.Level: Bachelor level with 3 to 5 years’ experienceExperience in logistics or supply chain, in an international environmentRequired Skills and QualificationsBachelor’s degree in related field required.Strong practical working experience with Logistics and Customs Operations in EU.In depth working experience in European wide shipping of cargo (both palletized and bulk) and all aspects associated with it, i.e. import, document flow, demurrage, equipment etc.Understands domestic and international shipping requirements.Fluent in English and French both verbally as written. Knowledge of any other European language is an asset.Effective Communicator: Strong written and verbal communication skills. Able to communicate effectively at all levels of the organization as well as with vendors.Team Player: demonstrated ability to build relationships and work effectively with people across functions and regions.Integrative Thinker: ability to use judgment and experience to look and take into account various aspects of the business processes and value chain to make recommendations and drive opportunities for cost optimization.Strong initiative and commitment.Problem Solver: a creative yet pragmatic problem solver. Methodical and hands-on, as well as detail-oriented. Excellent planning, execution, and project-management skills. Analytical mind: being able to identify and collect relevant data, to put relevant data in correlation, crunch it and visually display the results (excel pivot tables, power point).Ocean freight knowledge as well as International Trade Compliant and SAP knowledge are all assets.Assuring integrity of the logistic information is critical in order to manage the complexities of the business.Project work is a very important part of the role, and will give breadth and diversity to the day-to-day work contents
IT Data & Operations specialist - Verviers
Select, Liuege, Wallonia
FunctieomschrijvingYou coordinate the troubleshooting of the Warehouse Management System (WMS) to fix application issue impacting critical business processYou manage the third-party resolution activity for major IT Supply Chain Application (major incidents and problems) and participate to analysis of business issue (IT problem management) to identify root cause and provide quick workaround for first line of support.You provide the adequate support for critical Dataset and Dataflow to limit the impact on Business operation, especially for the Distribution Center (Supply Chain).You manage master data including creation, updates, deletion, commissioning and decommissioning of data sets.You help to develop reports and analysis in collaboration with the application and infrastructure teamsYou manage and design the reporting environment, including data sources, security, and metadata.You troubleshoot the reporting database environment and reports.You recommend and use tools and develop methods to support data integrity and normalization processYou evaluate changes and updates to data source production systems.You help to measure and warranty high performance of application database by developing smart monitoring scenario.You provide technical expertise on data storage structures, data mining, and data cleansing.You help to coordinate the delivery for the Warehouse Management System applicationProfiel5 years’ experience in IT similar role (Data analyst or Operation analyst or similar field)Demonstrated experience in handling large data sets and relational databasesExperience in Supply Chain is a plusIT SkillsHigh knowledge in SQL language and development tools.Ability to analyze existing tools and databases and provide software solution recommendations.Ability to translate business requirements into non-technical, lay terms.Ability to work with several reporting tools: SAP BO, POWER BI, Azure Data lake, Azure Data factory, MS SSRS.Good knowledge of database administration, especially MS SQL server.Good understanding of SQL server Integration Service (SSIS).Organisatie- en afdelingomschrijvingNotre client est une société internationale, leader mondial dans son secteur d'activité. Dans le cadre de son développement et de sa transformation numérique, notre client crée un nouveau poste et recherche un (e) IT Data & Operations Specialist/Analyste de données, spécialiste dans le suivi des opérations IT, idéalement avec expérience dans le secteur Supply Chain/Logistique (H/F). Ce poste nécessite une très bonne connaissance de l'anglais. Ce pourquoi la description de fonction ci-dessous est uniquement publiée en anglaisAanbodNotre client propose un CDI d'entrée. Vous travaillez dans une entreprise multiculturelle, innovante et dynamique. Le salaire est fonction de vos expériences et est assorti d'avantages extra-légaux (voiture, chèques-repas, assurances).Postulez rapidement!
IT Internship
SPIE, Wallonia
Informations générales IT Internship (réf. 2021-19409) SPIE Belgium aide ses clients d'une part à concevoir et réaliser leurs équipements techniques et d'autre part, à exploiter et assurer la maintenance de leurs installations. Chaussée de Louvain, 431 C 1380 Lasne Stage QUE FAIT IT Internship CHEZ SPIE ?What does a IT Intern do at SPIE Belgium ICS?Our teams support and facilitate the digital transformation of our corporate and enterprise customers all over Belgium. SPIE Belgium ICS designs, operates and integrates tailored ICT solutions in the areas of Workspace, IT Security, Datacenter & Cloud, Printing & Document Management and IP Connectivity.As an IT Intern you will begin your professional adventure at SPIE Belgium ICS. You will build the future of your career and you will continue to grow as an informatician and as a person. Here, you will be trained by our expert collaborators to finally become a technical specialist.How can you build your future at SPIE Belgium ICS ?At the beginning of your internship, you will have the opportunity to follow internal trainings provided by our senior engineers. With those you will be able to develop your IT knowledge and discover the new technologies we are working on. It will help you to build your future career. Depending on your motivation and skills you may be able to develop your own specific IT skills and earn a permanent contract.In which areas will you outperform?You will learn how to analyse and resolve incidents and problems, and execute changes in different IT environments.You will improve your troubleshooting skills that allow you to resolve incidents without breaching SLA.You will understand the importance of Knowledge Management, and contribute to this by writing and updating documentation and proceduresYou will learn from our experts and at the end of your internship you will be able to advise and provide quality technical expertise to our customersQU'EST-CE QUI VOUS REND TELLEMENT SPIE ?What makes you so SPIE?You are ambitious, eager to learn and open-minded. You have a real solution-oriented spirit. You are motivated by challenges and the achievement of your objectives. These qualities are of course in addition to all your IT knowledge, which is the essence of your job. You are in your last year in a bachelor's with an informatic orientation.You are fluent in French or Dutch.You have a good general knowledge of IT.You have good communication skills.You enjoy performing in new situations.You are enthusiast and curiousPOURQUOI CHOISIR SPIE ?Why choose SPIE?You are choosing a sustainable future, an exciting internship full of challenging assignments and projects, and opportunities for development in a family-like atmosphere with an employer who has already been certified "Top Employer" 14 times. SPIE is part of a strong European group that is building a better world of smart cities and efficient buildings, energies and industries. But that's not all. You can count on : The expectation of permanent contract.1800 colleagues who listen to you, help you and enjoy talking to you.A 'good morning' every dayAn integration process that will quickly put you at ease.An internship where you will be able to develop your talents and innovation on a daily basisAn internship where you can develop your expertise and skills with the support of our IT ExpertsThe opportunity to contribute to exciting projects in your region that you can be proud of!Make the difference and feel useful thanks to all the social projects we supportUNIR NOS DIFFÉRENCES :SPIE is committed to promoting diversity and wants to guarantee equal opportunities, equal treatment and equal access to our selection procedures. We encourage all people to apply for its job offers regardless of their origin, skin colour, gender, age, sexual orientation, philosophical conviction or disability.
Specialist, CMC Vaccines Mature Products
GSK, Wavre, Walloon Region, be
Your responsibilities:You coordinate the timely preparation of technical (CMC) regulatory documents for lifecycle activities and maintenance of registered vaccines, in accordance with the applicable regulatory & scientific standards, taking into account the evolving regulatory requirementsYou may provide regulatory advice and guidance to the Technical Life-Cycle Team (TLCT), Implementation Committee, Specification Committee, Technical Review Board and may provide regulatory support to their partners in Quality Control, Manufacturing, QA and Supply, with appropriate guidance from supervisor.You ensure adequate interaction and partnership with the Global Regulatory Lead’s team in order to support the regulatory filing, ensure adequate preparation of the content, ready for submission.You engage in CMC Subject Matter Expert activities. In a continuous improvement mindset, you will ensure regulatory compliance is maintained and share best-practices and learnings within the CMC Regulatory teams.Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Bachelor’s degree in Sciences or Medical Sciences with the necessary relevant experienceKnowledge of drug development, manufacturing, supply processes.Knowledge of worldwide CMC regulatory requirements.String communication skillsFluent EnglishPreferred Qualifications:If you have the following characteristics it would be a plus:Master’s degree or above in Chemistry, pharmacy, biological or closely related science advanced degree. Regulatory Affairs Certification (e.g. RAPS)Knowledge of vaccines/biological products manufacturing and supply processes. Can identify areas for personal professional growth in global regulatory affairs with appropriate support from line manageUnderstands internal/external CMC Regulatory environment.*Li-GSK
Specialist Clinical Labs Quality
GSK, Rixensart, Walloon Region, be
Responsible for providing fit-for-purpose quality partnership and oversight for Clinical Laboratory Sciences (CLS) in order to secure effective pipeline delivery and audits/inspections readiness.This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:In alignment with Clinical Labs Quality strategy and in collaboration with CLS:Provide fit-for-purpose quality oversight and quality partnership, taking into account the applicable internal and external quality standards (including ISO 9001:2015) and regulatory requirements (including GCLP), with the objective to secure effective pipeline delivery and regulatory submission approvals.Provide QA expertise, coaching and training to support CLS teams.Contribute to continuous improvement and Smart Risk-taking Quality culture.Ensure one voice Quality and efficient connection between Q4R&D and CLS.Ensure audit & inspection readiness and CAPA follow-up.Clinical Development and Testing:Maintain adequate clinical development project understanding to ensure fit-for-purpose and robust analytical testing methods, equipments, computerized systems and processes are in place, validated and maintained according to requirements.Through Quality oversight:Ensure data integrity and reliability. Ensure that Human Biological Samples are used according to Quality standards and Regulatory requirements.Risk, opportunity and issue management:Pro-actively identify quality and compliance risk/opportunity and manage these through the CLS and GSK Vaccines risk and opportunity management process.Ensure timely escalation of issues to management.Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Master's degree in Sciences or equivalent5+ years of experience in Pharma of Life Sciences industryRelevant experience in Quality in GxP environmentRelevant experience in Research & Development, preferably in Clinical LaboratoriesUnderstanding of Clinical DevelopmentDemonstrated influence and problem-solving skillsPreferred Qualifications:If you have the following characteristics, it would be a plus:Knowledge of GSK Vaccines processes and environment in terms of R&D and QualityDeep knowledge in Quality System regulation requirements covering GCLP, GCP, GLP, ISO 9001:2015.In depth knowledge of requirements in data integrityAbility to partner with R&D business:Courage to challenge where appropriateAbility to inspire, partner and coach the organization to improve performanceStrong networking and collaboration skills in a complex environmentAbility to engage others and operate a fair process in reaching decisionsStrong communication and presentations skillsGood knowledge of quality and risk management principles and toolsAbility to manage stakeholders and build relationships transversally across GSK Vaccines networkExcellent communication, presentation and facilitation skillsSmart risk-taking mindset
Automation Specialist
Lyreco, Herstal, Walloon Region, be
Job DescriptionAutomation SpecialistLyreco is een totaalleverancier in de B2B markt voor Office & Work Solutions, van papier en inktcartridges tot catering & hygiëne en persoonlijke beschermingsmiddelen. We zijn een multinational, actief in 42 landen verspreid over 4 werelddelen en marktleider in de Benelux.Om ons team te versterken, gaan wij op zoek naar een Customer Care Automation / IT Specialist.Hoe ziet jouw dag eruit?In deze functie zorg je ervoor dat IT oplossingen maximaal worden ingezet om minder manueel werk te hebben binnen Lyreco BeneluxAutomatiseren van manuele werkprocessen is je dagelijkse passie: je haalt energie uit het opzetten van informatica oplossingen die het werk versnellen en vereenvoudigenKlanten en collega’s helpen met het oplossen van problemen behoort tot je takenpakket om ervaring te houden met de operationele realiteitJe zorgt ervoor dat de digitale oplossingen voor customer care perfect werken (Zendesk, Genesys)Wie zoeken wij?Ondernemende collega met kennis van ITKennis programmering (automatiseringstools zijn een plus: powerautomate, automation everywhere, …)Basiskennis SAPFlexibele leerstijlResultaatgerichtGoede kennis van Nederlands/Frans (eventueel Frans/Engels)Communicatief vaardig, zowel mondeling als schriftelijkTeamspelerStressbestendigWat bieden wij?Een aantrekkelijk salaris.20 Vakantiedagen + 6 extralegale verlofdagen.Serieuze doorgroeimogelijkheden!Maaltijdcheques voor je dagelijkse lunch.Een hospitalisatieverzekering met een aantrekkelijke premie.De mogelijkheid om extra pensioen op te bouwen met een pensioenspaarrekening.Customer Care Automation / IT SpecialistLyreco est un fournisseur total sur le marché B2B de solutions pour le bureau et le travail, du papier et des cartouches d'encre à la restauration et l'hygiène et aux équipements de protection individuelle. Nous sommes une entreprise multinationale, active dans 42 pays sur 4 continents et leader du marché au Benelux.Nous sommes à la recherche d'un Customer Care Automation / IT Specialist pour renforcer notre équipe.A quoi ressemble votre journée ?Dans cette fonction, vous vous assurez que les solutions informatiques sont utilisées au maximum afin d’avoir moins de travail manuel au sein de LyrecoL’automatisation des processus de travail manuel est votre passion quotidienne : vous avez de l’énergie pour la mise en place de nouvelles solutions informatiques qui accélèrent et simplifient votre travailAider les clients ainsi que les collègues à résoudre des problèmes informatiques fait partie de vos tâches quotidiennes afin de maintenir l’expérience de la réalité opérationnelleVous vous assurez que les solutions digitales et numériques pour le département client fonctionnent parfaitement bien (Zendesk – Genesys)Qui recherchons-nous ?Vous êtes un collègue entrepreneur avec de très bonnes connaissances en ITVous avez la connaissance des programmations (les outils d’automatisation sont un plus : powerautomate, automatisation n’importe où)Vous êtes capable de développer en interne des solutions en informatique pour nos divers départementsConnaissances basiques de SAPStyle d’apprentissage flexibleVous êtes orienté résultatsVous avez de très bonnes connaissances du Néerlandais & du Français (éventuellement de l'Anglais)Vous avez un bon esprit d’équipeVous êtes résistant au stressQue proposons-nous?Un salaire attractif.20 jours de congés légaux et la possibilité de recev oir 7 jours de congés extra-légaux.De réelles opportunités de croissance !Des chèques-repas.Une assurance hospitalisation.La possibilité de se constituer une pension complémentaire grâce à un compte d'épargne retraite.
SUPPORT SPECIALIST - Pharmaceutical sector
Eyetech Solutions, Nivelles, Walloon Region, be
DescriptionSupport Specialist - Your responsibilities- In close collaboration with the IT team, you will carry out several tasks in order to define and implement solutions to detected problems- You will solve user incidents or those reported by the first line- You will be responsible for implementing maintenance plans, writing documentation, and installing new equipment on site
FREELANCE AWS SPECIALIST - LIEGE + 6 MONTH
Eyetech Solutions, Liège, Walloon Region, be
DescriptionFreelance AWS SPECIALIST - The role:Experienced working with container platforms like Kubernetes and Openshift.Experience building CI/CD pipelines.Strong relational database skills.Ability to deliver effective solutions to complex problems independently.Knowledge integrating Security tools.
FREELANCE AWS DevOps SPECIALIST- WAVRE + 1 YEAR
Eyetech Solutions, Wavre, Walloon Region, be
DescriptionFreelance AWS DevOps SPECIALIST- The role:Manage AWS cloud, accounts and services through automation and scripting.Advanced proficiency with running/deploying containers.Evaluate new technologies and make recommendations.Strong Linux infrastructure background.
IT Infrastructure Specialist
Proselect, Verviers
Notre client, reconnu dans son domaine et de renommée internationale s'adjoint des forces de proselect dans sa recherche d'un(e) : IT INFRASTRUCTURE SPECIALIST (H/F/X) Votre mission: Un technicien IT au cœur du terrain ! Rattaché au département IT, votre mission consiste à travailler sur les tâches locales liées aux systèmes d’information de notre mandant.  Dans ce cadre, vos objectifs sont les suivantes : •    Assurer un bon fonctionnement des systèmes d'information ainsi que leurs évolutions ; •    Définition et mise en place de stratégies globales en coopération avec l’équipe et votre responsable ; •    Gestion de la maintenance des infrastructures informatiques  ; •    Administration locale (gestion des utilisateurs, des demandes spécifiques, des licences, etc) ; •    Gestion de serveurs locaux et distants ; •    Gestion locale LAN, WAN, VPN ; •    Contact avec les supports externes et centraux ; •    Vous proposez des projets et optimalisations du support informatique. L'objectif est d’assurer le fonctionnement et l’efficacité maximale de l’entreprise en tenant compte de la sécurité et de la disponibilité la plus haute possible. Votre profil: Polyvalence et technicité !  •    Vous êtes diplômé d'un graduat dans le domaine informatique et avez des connaissances techniques liées au support et gestion des réseaux ou une première expérience similaire réussie dans le milieu de support IT ; •    Vous vous exprimez en français et avez de bonnes connaissances en anglais ; •    Team player, vous faites preuve d’un bon esprit d’équipe et êtes capable de travailler dans une grande structure (respect des règles, des horaires, des standards, des best practices) ; •    Votre esprit critique vous permet d’analyser et de résoudre avec sang-froid les problèmes techniques rencontrés ; •    Orienté clients, vous avez le contact facile et conseillez volontiers vos interlocuteurs ; Bagage technique souhaité: Windows Server (Files, Print, DHCP, DNS, DFS), WSUS,Active Directory, MS Exchange, MS SQL, IIS ; Windows 10 (Pro & IoT); Microsoft 365; VMware (vSphere), VEEAM ; Network LAN, WLAN, WAN, VLAN, Firewall, Switching(Cisco), IP teleponie (Cisco). Notre offre: Notre mandant vous offre un travail passionnant sous contrat à durée indéterminée et ce, au sein d'une organisation en pleine croissance où vous prendrez une part active dans une équipe dynamique. proselect gère cette mission en exclusivité. Tout candidat intéressé est donc invité à postuler exclusivement via le bouton "Postuler". Votre candidature sera traitée avec rapidité et confidentialité.
Quality Assurance CSV specialist
Thermo Fisher Scientific, Seneffe, Walloon Region, be
MISSION Le QA « CSV specialist »t est le garant de l’état qualifié des système informatisé et l’interlocuteur privilégié de l’IT. Il assure le respect et l'application de la politique assurance qualité définie par l'entreprise dans l'ensemble des processus qui lui sont soumis.DOMAINES DE RESPONSABILITESGestion OpérationnelleAssister le Responsable AQV dans toutes les tâches de l’AQV afin de veiller au respect des processus et outils de gestion sur le terrain.Être le QA référent du service informatique, des services opérationnels, et du groupe lors que cela concernant les systèmes informatisés et l’infrastructure IT.Participer à la rédaction et à l’approbation des plans et rapports liés à la qualification (requalification) & validation URS, FAT, SAT, Analyse de risque, IQ ,OQ, PQ , des systèmes informatisés.Contrôler le bon déroulement des opérations de qualification & validation sur le terrain afin d’assurer que les systèmes sont opérationnels et en état de validité permanente.Gère les revues périodiques d’un point de vue CSVApprouver les SOP liées aux systèmes informatisés. Assurer que le personnel est formé à l’utilisation de ces équipements.Participer à toutes les réunions, AIC de suivi des systèmes informatisés & qualificationGérer les déviations, demandes de modification, dérogations, CAPA, Avis PM liées aux activités de systèmes informatisés & qualification en relation étroite avec les autres domaines de l’AQ et les autres départements.Participation en tant d’auditeur interneParticiper aux inspections et audit externes (clients, groupes, autorité)Participation ponctuelle aux audits fournisseurs et prestataire de serviceExcellence opérationnelleAppliquer les outils et les méthodes définis par le groupeFaire des propositions d’améliorations de process et procéduresAlimenter des indicateurs de performanceParticiper aux AICsAppliquer et soutenir la politique 5S dans son équipe Sécurité Respecter et faire respecter les normes de sécurité & biosécurité en vigueurQualité Garantir la qualité documentaireRespecter le système qualité mis en place sur le siteAssurer des missions périphériques dans le domaine de ses compétences, à la demande de sa hiérarchie.INTERACTIONS ITOpérationsGroupePREREQUISFormation supérieure de type Baccalauréat ou Master en biologieConnaissance des cGMPConnaissance en système informatisé / Data intégritéConnaissance de SAPExpérience en milieu biopharmaceutique de minimum 5 ansAnglaisCOMPETENCESTechniques/MétierSAPAffinité avec les systèmes informatisésFamilier avec les processus qualitésConnait l’annexe 15 et 11 de l’eudralex et le 21CFR part11ExcelComportementalesAssertivitéRigoureuxEsprit de synthèseCapable de challengerVision risque corruption de donnée / produit / patientFonction CritiqueBack-up de QA Technics Qualification & Validation SpecialistQA Technics Qualification & Validation Manager
RC 364624 : LGG Air Network Specialist
FedEx Express EU, Grâce-Hollogne, Walloon Region, be
:Key activities:Capacity managementTo plan, coordinate and supervise the capacity utilization of outbound flights as per defined priorities in order to achieve highest possible load factor onto aircraftCommunicate amount and type of ULD’s per product to be used per flight to HUB Ops and CTOEnsure the priority settings are respected for uplift of materialRecord and report any offloads to required channels to allow status updatesSupervise any offloaded freight is being stored in the designated areaLiaise with LGG GLN for contingency commercial movements for core express productsOn time performance managementTo supervise and control Critical Timings are respected in respect of buildup of freight by HUB Ops and/or CTO and also the freight movements from warehouse to aircraft in liaison with ramp handlingEnsure the compliance with the agreed SLA for freight cut offs and report / follow up on non-compliancesEnsure paperwork pouches are put on board in timeCoordinate with HUB, CTO and ramp to swift transfers of uld’s up to aircraftInbound cargo movement managementTo ensure the inbound cargo is expedited according to the SLA agreed with CTOEnsure cargo material and cargo paperwork is handed over swiftly to CTO upon arrival in liaison with ramp handlerPrepare and communicate the outbound truck planning in liaison with the CTOProcess supervision To supervise and monitor the deployment operational policies and procedures in order to ensure the consistency, efficiency and quality of internal and external customers and stakeholdersEnsure correct implementation of existing and new divisional operation structures, policies and processes in respect of buildup, labelling, data captor, AVSEC and airline paperwork commutingReport any anomalies to responsible stakeholders for corrective actions Flight documentation and Control To supervise and control in order to ensure the paperwork is issued as per the legal, customs and airline requirements and connected with the relevant flightEnsure paperwork for express and cargo is handed over/ collected from HUB Ops and CTO from inbound and outbound flights in liaison with ramp handler Ensure the Mawb’s (Master Air Waybill) made for express are per company and airline requirements - follow up anomalies with hub office processingEnsure the Mawb’s for general cargo are per company and airline standardsCorporate Responsibility & Health & SafetyTo comply with local, national legislation, Health & Safety and Environment regulations in order to maintain a safe working environment for self and all the depot employees.Participate in the corporate initiativesRespect the H&S proceduresRespect the H&S instructionsAct & work safelyMake use of the PPE (personal protective equipment) provided by the companyReport possible risks to the hierarchySelf-behaviourDisplay a positive, open and cooperative behaviour in order to facilitate a good relationship inside and outside the department, avoid and help to solve conflicts.Be flexiblePreferred Experience/Knowledge:Mandatory skillsExcellent computer skills (Word, Excel, Power Point)Bilingual French/EnglishMinimum secondary educationPreferred Experience and KnowledgeProven experience and knowledge of airfreight , AVSEC , DG , customs regulations is an assetExperience in a multinational company and working with different culturesExcellent level of English and French (written and spoken)Functional & Behavioral competenciesGood analytical skillsGood communication skillsBeing able to “manage” people outside his direct controlRecruitment process:Check CCT /Steps (for internal candidates)Résumé screeningPhone screeningPanel Interview including a presentationEvery step is eliminatoryFedEx was built on a philosophy that puts people first, one we take seriously. We are an equal opportunity employer and we are committed to a diverse and inclusive workforce in which we provide growth opportunities for allOur CompanyFedEx Express is one of the world's largest express transportation companies and has consistently been selected as one of the top 10 World’s Most Admired Companies by "Fortune" magazine. Every day FedEx delivers for its customers with transportation and business solutions, serving more than 220 countries and territories around the globe. We can serve this global network due to our outstanding team of FedEx team members, who are tasked with making every FedEx experience outstanding.Our PhilosophyThe People-Service-Profit philosophy (P-S-P) describes the principles that govern every FedEx decision, policy or activity. FedEx takes care of our people; they, in turn, deliver the impeccable service demanded by our customers, who reward us with the profitability necessary to secure our future. The essential element in making the People-Service-Profit philosophy such a positive force for the company is where we close the circle, and return these profits back into the business, and invest back in our people. Our success in the industry is attributed to our people. Through our P-S-P philosophy, we have a work environment that encourages team members to be innovative in delivering the highest possible quality of service to our customers. We care for their well-being, and value their contributions to the company.Our CultureOur culture is important for many reasons, and we intentionally bring it to life through our behaviors, actions and activities in every part of the world. The FedEx culture and values have been a cornerstone of our success and growth since we began in the early 1970’s. While other companies can copy our systems, infrastructure and processes, our culture makes us unique and is often a differentiating factor as we compete and grow in today’s global marketplace.
RC 364624 : LGG Air Network Specialist
FedEx, Grâce-Hollogne, Walloon Region, be
Empresa: FedEx Express EUNúmero de solicitud de trabajo: RC364624Ubicaciones:Rue de l'Aéroport 90Grace-Hollogne, BélgicaHorarios semanales programados: 38Tipo de trabajador: RegularFecha de publicación: 11-May-2021Fecha de cierre: 31-August-2021Trabajo familiar: FXE-EU: Air Network Specialist (ID)Resumen de posición:Key activities:Capacity managementTo plan, coordinate and supervise the capacity utilization of outbound flights as per defined priorities in order to achieve highest possible load factor onto aircraftCommunicate amount and type of ULD’s per product to be used per flight to HUB Ops and CTOEnsure the priority settings are respected for uplift of materialRecord and report any offloads to required channels to allow status updatesSupervise any offloaded freight is being stored in the designated areaLiaise with LGG GLN for contingency commercial movements for core express productsOn time performance managementTo supervise and control Critical Timings are respected in respect of buildup of freight by HUB Ops and/or CTO and also the freight movements from warehouse to aircraft in liaison with ramp handlingEnsure the compliance with the agreed SLA for freight cut offs and report / follow up on non-compliancesEnsure paperwork pouches are put on board in timeCoordinate with HUB, CTO and ramp to swift transfers of uld’s up to aircraftInbound cargo movement managementTo ensure the inbound cargo is expedited according to the SLA agreed with CTOEnsure cargo material and cargo paperwork is handed over swiftly to CTO upon arrival in liaison with ramp handlerPrepare and communicate the outbound truck planning in liaison with the CTOProcess supervision To supervise and monitor the deployment operational policies and procedures in order to ensure the consistency, efficiency and quality of internal and external customers and stakeholdersEnsure correct implementation of existing and new divisional operation structures, policies and processes in respect of buildup, labelling, data captor, AVSEC and airline paperwork commutingReport any anomalies to responsible stakeholders for corrective actions Flight documentation and Control To supervise and control in order to ensure the paperwork is issued as per the legal, customs and airline requirements and connected with the relevant flightEnsure paperwork for express and cargo is handed over/ collected from HUB Ops and CTO from inbound and outbound flights in liaison with ramp handler Ensure the Mawb’s (Master Air Waybill) made for express are per company and airline requirements - follow up anomalies with hub office processingEnsure the Mawb’s for general cargo are per company and airline standardsCorporate Responsibility & Health & SafetyTo comply with local, national legislation, Health & Safety and Environment regulations in order to maintain a safe working environment for self and all the depot employees.Participate in the corporate initiativesRespect the H&S proceduresRespect the H&S instructionsAct & work safelyMake use of the PPE (personal protective equipment) provided by the companyReport possible risks to the hierarchySelf-behaviourDisplay a positive, open and cooperative behaviour in order to facilitate a good relationship inside and outside the department, avoid and help to solve conflicts.Be flexiblePreferred Experience/Knowledge:Mandatory skillsExcellent computer skills (Word, Excel, Power Point)Bilingual French/EnglishMinimum secondary educationPreferred Experience and KnowledgeProven experience and knowledge of airfreight , AVSEC , DG , customs regulations is an assetExperience in a multinational company and working with different culturesExcellent level of English and French (written and spoken)Functional & Behavioral competenciesGood analytical skillsGood communication skillsBeing able to “manage” people outside his direct controlRecruitment process:Check CCT /Steps (for internal candidates)Résumé screeningPhone screeningPanel Interview including a presentationEvery step is eliminatoryFedEx se fundó siguiendo la filosofía de que las personas son lo principal, una actitud que nos tomamos muy en serio. Ofrecemos oportunidades de empleo equitativas y estamos comprometidos con una plantilla inclusiva y diversa con oportunidades de desarrollo para todos.Nuestra compañía FedEx Express es una de las compañías de transporte exprés más grandes del mundo y ha sido elegida sistemáticamente como una de las 10 empresas más admiradas del planeta por la revista Fortune. Cada día FedEx cumple las expectativas de sus clientes con soluciones comerciales y de transporte, y ofrece servicio en más de 220 países y territorios en todo el mundo. Logramos prestar servicio con esta red internacional gracias a los excelentes miembros que componen el equipo de FedEx, encargados de que cada experiencia con FedEx sea excepcional.Nuestra filosofíaLa filosofía Personas-Servicio-Beneficio describe los principios que rigen todas las decisiones, políticas o actividades de FedEx. FedEx se preocupa por las personas que integran su plantilla y ellas, a su vez, ofrecen el impecable servicio exigido por nuestros clientes, que nos proporcionan el beneficio necesario para garantizar nuestro futuro. El elemento esencial que convierte a la filosofía Personas-Servicio-Beneficio en la fuerza positiva que es para la compañía radica allí donde cerramos el círculo y devolvemos dichos beneficios al negocio e invertimos en nuestra gente.Nuestro éxito en el sector se debe a nuestros trabajadores. Mediante la filosofía Personas-Servicio-Beneficio, nuestro entorno de trabajo anima a que los miembros de los equipos sean innovadores a la hora de ofrecer un servicio de la mayor calidad posible a nuestros clientes. Nos preocupamos por su bienestar y valoramos sus aportaciones a la compañía.Nuestra culturaNuestra cultura es importante por muchas razones y hacemos que cobre vida deliberadamente a través de nuestro comportamiento, nuestras acciones y nuestras actividades en cada rincón del mundo. La cultura y los valores de FedEx llevan siendo la piedra angular de nuestro éxito y expansión desde nuestros comienzos a principios de la década de los 70. A pesar de que otras compañías puedan copiar nuestros sistemas, infraestructura y procesos, nuestra cultura nos hace únicos y es, con frecuencia, un factor diferenciador en nuestra competencia y desarrollo en el mercado internacional actual.
Sr Quality Systems Specialist
Medtronic, Ottignies-Louvain-la-Neuve, Walloon Region, be
Senior Quality Systems Specialist Careers that Change LivesAt Medtronic, we strive without reserve for the greatest possible reliability and quality in our products and processes. As part of the EMEA Quality System, Medtronic Service & Repair EMEA Quality has established the quality processes that cover technical service incl. customer care, service centers and field service which apply throughout the EMEA (Europe, Middle East and Africa) region. The service center in Heerlen supporting Western Europe, all field service within S&R EMEA and all S&R EMEA customer care are certified according ISO 13485 and ISO 9001. We are currently looking for a (Senior) Quality Systems Specialist to maintain and improve our Quality System. A Day in the LifeYou contribute to, maintain and improve the S&R EMEA Quality System by establishing the quality processes and supporting the in-country Service & Repair teams and process owners with the implementation and maintenance of these processes. Next to this, you provide advice and act as SME on ISO standards, Regulatory, and Corporate quality requirements, you prepare and follow-up both internal and external audits, you support/review preventive and corrective actions, you support with the preparation and follow-up of our biannual Quality Management Reviews and participate in specific Quality related projects. We offer you a position that allows you to be active throughout different parts of the organization and take the lead in different S&R QA processes. You represent the S&R QA team and are in direct contact with different Service & Repair stakeholders and process owners throughout the EMEA region, and with EMEA Quality. You are expected to work independently on your task and will be part of the S&R EMEA Quality Team. Your main tasks and responsibilities include:• Provide Quality Systems advice to process owners within the scope of the S&R EMEA QMS;• Act as SME on the applicable ISO standards, Regulatory, Corporate or other Quality Requirements;• Act as a delegate in one or more S&R QMS processes;• Develop and provide training on applicable quality related subjects;• Prepare, participate in and follow-up internal and external audits;• Analyze data to identify trends and opportunities for improvement on quality aspects;• Support improvement projects;• Support with gathering the input for, attend and follow-up our bi-annual Quality Management Reviews;• Investigating root cause of quality issues and approving corrective/preventive actions to prevent reoccurrence. Do you have what it takes:• Bachelor Degree in Health Sciences, Health Policy, Business or similar;• Preferably 1-3 years of relevant working experience in a quality role in a highly-regulated environment (preferably in medical technology/logistical operational environment, regulatory affairs);• Excellent command of the English both spoken and written;• To be successful in this role you recognize yourself as a:• Self-starter, and a decision maker;• You have a strong passion for quality and continuous improvement;• you show a hands-on and result oriented approach to the application of quality tools;• You are a distinct standout colleague, who’s able to establish relationships with colleagues in other countries and departments;• Handling several tasks, priorities and projects at once poses no problem for you and you can work well in a high pace environment;• Your excellent communication and presentation skills enable you to energize your audience and inspire change. We OfferIn our 5th Tenet of our Mission we recognize the personal worth of employees by providing an employment framework that allows personal satisfaction in work accomplished, security, advancement opportunity, and means to share in the company's success. Also a competitive package is of course part of that. We offer a competitive salary and benefits package to all our employees:• Flexible working environment;• Annual Incentive Plan % depending on company results;• Pension scheme and group discount on healthcare insurances;• Training possibilities via Cornerstone/Harvard Manage Monitor/GetAbstract;• Employee Assistance Program and Recognize! (our global recognition program). Your Answer Is this the position you were waiting for? Then please apply directly via the apply button! About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life.We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives help us shape the future.Founded in 1949 as a medical repair company, we're now among the world's largest medical technology, services and solutions companies, employing more than 86,000 people worldwide, serving physicians, hospitals and patients in over 155 countries. Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your own career. Join us in our commitment to take healthcare Further, Together. Additional Information Posting Date: Apr 29, 2021 Travel: No
Quality Assurance CSV specialist
Thermo Fisher Scientific, Seneffe, Wallonia
MISSION Le QA « CSV specialist »t est le garant de l’état qualifié des système informatisé et l’interlocuteur privilégié de l’IT. Il assure le respect et l'application de la politique assurance qualité définie par l'entreprise dans l'ensemble des processus qui lui sont soumis.DOMAINES DE RESPONSABILITESGestion OpérationnelleAssister le Responsable AQV dans toutes les tâches de l’AQV afin de veiller au respect des processus et outils de gestion sur le terrain.Être le QA référent du service informatique, des services opérationnels, et du groupe lors que cela concernant les systèmes informatisés et l’infrastructure IT.Participer à la rédaction et à l’approbation des plans et rapports liés à la qualification (requalification) & validation URS, FAT, SAT, Analyse de risque, IQ ,OQ, PQ , des systèmes informatisés.Contrôler le bon déroulement des opérations de qualification & validation sur le terrain afin d’assurer que les systèmes sont opérationnels et en état de validité permanente.Gère les revues périodiques d’un point de vue CSVApprouver les SOP liées aux systèmes informatisés. Assurer que le personnel est formé à l’utilisation de ces équipements.Participer à toutes les réunions, AIC de suivi des systèmes informatisés & qualificationGérer les déviations, demandes de modification, dérogations, CAPA, Avis PM liées aux activités de systèmes informatisés & qualification en relation étroite avec les autres domaines de l’AQ et les autres départements.Participation en tant d’auditeur interneParticiper aux inspections et audit externes (clients, groupes, autorité)Participation ponctuelle aux audits fournisseurs et prestataire de serviceExcellence opérationnelleAppliquer les outils et les méthodes définis par le groupeFaire des propositions d’améliorations de process et procéduresAlimenter des indicateurs de performanceParticiper aux AICsAppliquer et soutenir la politique 5S dans son équipe Sécurité Respecter et faire respecter les normes de sécurité & biosécurité en vigueurQualité Garantir la qualité documentaireRespecter le système qualité mis en place sur le siteAssurer des missions périphériques dans le domaine de ses compétences, à la demande de sa hiérarchie.INTERACTIONS ITOpérationsGroupePREREQUISFormation supérieure de type Baccalauréat ou Master en biologieConnaissance des cGMPConnaissance en système informatisé / Data intégritéConnaissance de SAPExpérience en milieu biopharmaceutique de minimum 5 ansAnglaisCOMPETENCESTechniques/MétierSAPAffinité avec les systèmes informatisésFamilier avec les processus qualitésConnait l’annexe 15 et 11 de l’eudralex et le 21CFR part11ExcelComportementalesAssertivitéRigoureuxEsprit de synthèseCapable de challengerVision risque corruption de donnée / produit / patientFonction CritiqueBack-up de QA Technics Qualification & Validation SpecialistQA Technics Qualification & Validation Manager
System Architect Cloud Specialist
Select, Lasne, Wallonia
FunctieomschrijvingVotre missionVous êtes responsable de l'organisation, de la planification, de l'exécution et de l'amélioration d'un large éventail de produits livrables dans des environnements Cloud et locaux :• Gestion de la plate-forme Windows Server en général (de la livraison du serveur à la mise hors service)• Déploiement de logiciels et correctifs de sécurité de la plate-forme• Gestion et organisation de l'évolution du parc• Gestion quotidienne de la base de serveurs installée (contrôles de qualité, respect des normes, etc.)• Gestion de l'infrastructure antivirus et des mises à jour antivirus sur les serveurs Windows• Gestion de la plateforme de messagerie Exchange et/ou O365• Gestion des plateformes de virtualisation• Migration de la plateforme existante vers un nouvel environnement local ou migration vers un environnement CloudProfielVotre profil• Vous avez une expérience confirmée dans la gestion et la prise en charge d'environnements de serveurs Windows complexes et de grande taille (Windows 2012, 2016, 2019).• Vous parlez couramment le français et le néerlandais. Vous détenez également une bonne connaissance de l'anglais.• Vous détenez une expérience confirmée dans l'installation et la gestion d'environnements :o Exchangeo Office 365o Azure• Vous avez de l'expérience dans l'utilisation d'une infrastructure de déploiement• Vous témoignez d'une très bonne connaissance d'un ou plusieurs de ces domaines: matériel HP/DELL/LENOVO, infrastructure antivirus, virtualisation, backup …• Vous connaissez les solutions de clustering et d'équilibrage de chargeOrganisatie- en afdelingomschrijvingEn tant qu’intégrateur, expert en transformation Cloud et fournisseur de Managed Services, la division IT conçoit, intègre, opère et finance des solutions ICT complètes et modulables dans 5 domaines d’expertise technologique : Smart city, e-fficient buildings, Industry services et Energies.AanbodOffre- Un package salarial compétitif assorti d'un véhicule de fonction, Smartphone/ Laptop, chèques-repas, assurance groupe et hospitalisation.- Une entreprise reconnue TOP employer- Des certifications et nombreuses formations