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12 resultaten voor Wetenschap in Hoeilaart binnen een straal van 30 km
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Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - You will ensure the follow-up of productions; this involves monitoring chemical synthesis operations through dossier review, managing deviations, and following change control (review of change control). Daily contact with production is required. Votre profil * Bachelor's degree in Sciences * Minimum 3-5 years of experience in Quality Assurance in a regulated pharmaceutical environment or other life science or health-related field. * Experience in pharma is a must (must quickly become autonomous): experience with chemical/pharmaceutical production, development, and/or regulatory requirements, including knowledge of production best practices in the pharmaceutical industry.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Brabant Wallon – Contracting - Vos responsabilités * Technical expert in the establishment of robust, fit for purpose injectable drug product manufacturing processes from toxicology studies or first in human until BLA approval. * Define and select drug product manufacturing processes and parameters for clinical manufacture. * Cooperate with a wide range of internal and external stakeholders, including contract manufacturing organizations, as part of a project team. * Design and execution of lab studies in relation to drug product development activities, capture and analyze data and author related documentation (write-ups, protocols, reports (eg filter selection and sizing, target fill volume assessment, compatibility assessments, clinical blinding, etc).
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Work closely with Clinical Manufacturing Teams to ensure that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way. * More specifically, provide quality support for qualification and validation activities related to Clinical Manufacturing activities like facilities cleaning processes, viable and non-viable environmental monitoring, equipment and system qualification/validation * Drive the continuous QA improvement process. Ensure adequate documentation processes and systems are available and followed for development projects (SOPs / Prot
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Establish and build a network with the company key stakeholders in relation to Internal and External MSAT for Bio Drug Substances and Drug Products. * Troubleshooting and ensure issues are resolved in accordance with policies and procedures * Process improvement and life cycle management strategy within regulatory file boundaries * Process industrialization and Technical transfers within commercial manufacturing facilities * Complex investigations and CAPA plans implementation * Process validation oversight and continuous process verification (CPV) * Analytical method transfer and troubleshooting support. * Build, establish and develop a governance model and process for Quality oversight of Internal and External MSAT for Bio Drug S
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Business IT Developer - Power BI
Business IT Developer - Power BI
Nationale Bank van België NV / Banque Nationale de Belgique SA
Berlaimontlaan 14, 1000 Brussel
Thuiswerken mogelijk
Nationale Bank van België NV / Banque Nationale de Belgique SA * Berlaimontlaan 14, 1000 Brussel * Vast contract, onbepaalde tijd * Thuiswerken mogelijk - Introductie - De Nationale Bank van België (NBB) is in volle digitale transformatie. Om deze te verwezenlijken is een goede samenwerking tussen business en IT cruciaal. Business partnering staat dan ook centraal in onze IT-strategie. De NBB biedt veel nieuwe IT-mogelijkheden (cloud/data/automation) die we kunnen inzetten voor onze stakeholders. Als Business IT Developer – Power BI zal je onze dienst IT Business Partnering & Applications versterken en zal je mee innovatieve technologische oplossingen uitwerken om business objectieven te bereiken. In je job ben je omringd door echte experten, werk je in een mensgerichte omgeving met veel technologische uitdagingen en zijn er tal van mogelijkheden om jezelf verder te o
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Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Walloon Brabant - Your responsibilities * The GMP oversight of different laboratories and production pilots, including packaging, and outsourcing * The GSP oversight (non- GMP activities) of different development entities, located on the Braine site (BE), the Slough site (UK) and the Monheim site (DE). * Drive continuous quality improvement process, ensuring that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way. * Provide support for qualification and validation activities of the different laboratories and production pilots.
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Masterdiploma met focus (bij voorkeur binnen ingenieurswetenschappen, rechten, economie...)
Business Analyst - specialisatie IT - Effecten (V/M/X)
Business Analyst - specialisatie IT - Effecten (V/M/X)
Nationale Bank van België NV / Banque Nationale de Belgique SA
Brussel
Thuiswerken mogelijk
je beschikt, bij voorkeur, over een master in (toegepaste) economische wetenschappen, handelsingenieur, aangevuld met een IT-opleiding of een master IT, aangevuld met een opleiding in financieel-economische domeinen of je hebt een gelijkwaardige ervaring
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Kom op tegen Kanker VZW * SINT-JOOST-TEN-NODE * Vast contract, onbepaalde tijd * Voltijds - Introductie - Wil jij je IT-expertise inzetten voor een maatschappelijk doel? Bij Kom op tegen Kanker bouwen we aan een innovatieve digitale toekomst. Daarom zoeken we een Digital platform engineer om ons team te versterken. Iemand die ervoor zorgt dat onze digitale tools optimaal functioneren en naadloos aansluiten op onze missie. Klinkt dit als jouw volgende uitdaging? Lees verder! Jouw verantwoordelijkheden - Wat ga je doen? Als Digital platform engineer ben je verantwoordelijk voor de implementatie, configuratie en het beheer van onze digitale platformen, zoals Salesforce en andere werkplektools. Je zorgt ervoor dat deze systemen optimaal functioneren en perfect aansluiten op de behoeften van de organisatie. Daarnaast werk je aan custom ontwikkeling, waarbij je maatwerkoplo
Seascape Belgium bvba * ELSENE * Contract duration unspecified * Full Time - Introduction - We are looking to engage enthusiastic and motivated individuals for an internship in support of a range of communication and outreach activities for some of our key projects and initiatives (see The traineeship will involve on the job learning by taking on tasks in support of initiatives such as EU4Ocean, the European Atlas of the Seas and projects related to the development of European Digital Twin of the Ocean. The EU4Ocean Coalition connects diverse organisations, projects and people across Europe that contribute to ocean literacy and the sustainable ocean management. It includes three communities: the EU4Ocean Platform for organisations and individuals, the Youth4Ocean Forum and the Network of European Blue Schools.
Neoscan Bv * MECHELEN * Contract duration unspecified * Full Time - Your tasks * As part of a team, designing and implementing advanced software for scientific instrument control, 3D reconstruction, image processing and realistic 3D-visualization. * Join the product development team up to final system realization. * Architect/design/code new features for 3-dimensional imaging and measurements independently. Your profile - University degree (MD, Ph.D., Eng.) in science, computer technologies. In-depth knowledge and experience in software development under Windows environments. programming skills using a wide variety of tools, including Microsoft Visual C++ / Visual Studio and other development tools. Experience in programming of 3D-graphics withOpenGL, GLSL, experiences in CUDA and in image analysis are plus points. Good knowledge of English.
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Delta Light * Belgium * Contract duration unspecified * Full Time - Delta Light HQ - Wevelgem - Möchten Sie Teil eines international tätigen Unternehmens mit fantastischen KollegInnen werden, in dem Ihre Ideen gehört und Ihre Talente gefördert werden? Klicken Sie hier, um sich direkt zu bewerben. Gesellschaft >Incorporated in Belgium in 1989 by business manager and designer Paul Ameloot, today Deltalight has developed to become the market leader and trendsetter in architectural lighting. Presenting innovative lighting designs, the company is recognised throughout the world for its subtle blend of ambiance, elegance, functionality, and design, both in interior and exterior lighting. The future of Deltalight is guaranteed with Peter and Jan Ameloot joining their father at the helm of the company, bringing additional dynamism and ambition to the team.
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Proven experience in data validation, preferably in a regulated environment. * Validate the integrity of transferred and transformed data in the new system. * Draft and execute validation protocols (tests, reports, documentation). * Collaborate with IT and business teams to guarantee data accuracy and consistency. * Manage a backlog of dashboards awaiting validation and ensure effective follow-up. * Strong proficiency in SQL for executing tests and validating data. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Define User Requirement Specifications (URS) and ensure compliance. * Communicate with various (IT, Business, QA, QC). * Be proactive in coordinating ta
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The Vulnerability Analyst will be responsible for conducting vulnerability assessments, identifying system weaknesses, and recommending remediation strategies to minimize risk exposure. * Experience Level: Medior-level Vulnerability Analyst with proven experience in Cyber Security-related activities, specifically in vulnerability analysis. * Conduct vulnerability assessments to identify, analyze, and mitigate security risks. * Lead team meetings to streamline the vulnerability remediation process, ensuring efficient communication and timely resolution of security issues. * Conduct security awareness training for various teams, providing actionable guidance on vulnerability remediation and explaining potential impacts. * Generate and analyze weekly
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We are looking for a Project Manager to support the development of our hydrogen production projects in Flanders and Wallonia. As part of Virya Energy's hydrogen activities, you'll join a specialized team developing a growing portfolio of hydrogen production plants across Belgium and the Netherlands, with ambitions to expand further. We combine production development with innovative infrastructure solutions through DATS 24's refuelling network, while actively shaping the hydrogen market by establishing strategic partnerships with off takers. This unique position allows us to drive the entire hydrogen value chain forward, from production to end-user applications. * Lead and coordinate projects from concept to completion. * Monitor
Partner with QA and CMC Development/DCS colleagues to identify and mitigate Compliance risks, resolve potential regulatory observations. * The GSP oversight (non- GMP activities) of different development entities, located on the Braine site (BE), the Slough site (UK) and the Monheim site (DE). * Drive continuous quality improvement process, ensuring that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way. * Coordinate the development local instructions, liaise with key stakeholders in order to maintain common practices with regards to “issued copy” within development enti
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Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Département In vivo Pharmacologie - spécialisé dans les études in vivo, études de comportements sur différents rongeurs principalement souris et rats * Collectes de tissus, administration de composés et check effet sur le comportement des animaux * Préparation des réactifs et gestion du laboratoire - Votre profil * Master ou Doctorat en Sciences ou équivalent * Au moins un an d'expérience In vivo (meurins) * Titulaire du Felasa B * Connaissances en Excel * Excellentes compétences en Anglais - Notre offre - Jefferson Wells vous propose un contrat permanent en tant que consultant avec un package salarial attractif et vous donnera accès à des formations sur des sujets techniques ainsi que sur les soft skills. Nous serons votre partena
Experis is seeking a talented Data Expert to join the ICT Business Intelligence team of our client. Are you passionate about turning operational data into actionable insights? You will be the bridge between data needs and effective solutions, working closely with key stakeholders to understand their reporting challenges. Your goal is to transform complex data into visually engaging and easily understandable reports that make decision-making smoother and more efficient. * A keen eye for data accuracy and a genuine passion for transforming numbers into valuable insights. Experis * IXELLES / ELSENE * Contract duration specified * Full Time - Do you thrive in environments where your work drives tangible improvements and boosts efficiency? Your responsibilities - In this pivotal role, you
As a Drug Product Expert, you will act as key enabler supporting the advancement of Pharma Science's Science & Technology and Innovation projects by leveraging own area of expertise to functional initiatives and contribute to PS transversal initiatives. * Senior expert in clinical DP development accountable for leading and running assigned project work packages, ranging from clinical formulation orientation work for FIH study up to commercial registration and launch for the development pipeline and as part of the life cycle management of commercial brands. * To ensure process robustness, validation and transfer of NCEs and Lifecycle management of mature product manufacturing process and technologies to commercial launch site. * To perform clinical formulation orientation work in collaboration with Non-Clinical Formula
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Senior Information Security & Quality Officer (GRC Focus) As part of a small and dynamic team, you will focus on maintaining and enhancing cybersecurity and quality frameworks, ensuring regulatory compliance, and mitigating risks related to information security and business processes. * Ensure compliance of local Quality and Information Security Management Systems (QMS & ISMS) with international standards and regulatory frameworks (ISO 27001, ISO 9001, NIS/NIS2, NIST, etc.). * Coordinate awareness programs and training on information security, risk management, and compliance. * Minimum of five years of experience in information security governance, risk management, IT audit, or compli
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * S'assurer du respect cGMP. * Participer activement à la préparation des lots de process performance qualification (PPQ). * Revoir et approuver les dossiers de lot de production en version papier et électronique. * Participer à la gestion/revue/approbation des déviations. * Participer à la gestion/revue/approbation des CAPA. * Participer à la gestion/revue/approbation des change controls. * Revoir et approuver les protocoles et rapports de validation (CIP/SIP/EM/Thermal mapping). * S'assurer que les risques/non conformités identifiées sont traités de manières adéquates et remontés dans les temps. Votre profil * Diplômé(e) de l'enseignement supérieur de type Bachelier ou Master (biotechnologie, pharmacie, etc.). * Bilingue Français e
As an Analytical Development – Document Specialist, your mission is to write and review scientific documents related to the stability and comparability of products in clinical development, primarily in phase 3. * Proficiency in analytical techniques (HPLC, UPLC, etc.). * Previous experience in stability or analytical validation (an asset). Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Write stability and comparability protocols and reports. * Analyze and review scientific data to identify potential outliers. * Ensure data consistency and accuracy before submission to regulatory authorities. * Collaborate with and external . * Contribute to the continuous impro