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77 resultaten voor Wetenschappen in Elsene 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 - 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. * 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 improvement of documentation processes. Votre profil * Master's degree in Chemistry, Biochemistry, or a related field. * Minimum of 3 years' experience in the pharmaceutical, biotechnology, or related industry. * Excellent scientific writing skills in E
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Je hebt een Master in ingenieurswetenschappen of exacte wetenschappen op zak, of gelijkwaardige ervaring, en bent erkend als milieucoördinator type A.
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Hologic * Zaventem * Tijdelijk werk, interim, projectbasis * Voltijds - We're an innovative medical technology company whose purpose is to enable healthier lives everywhere, every day. While we discover and develop groundbreaking products and services that benefit everyone, we are especially passionate about those that advance women's health and well-being. This allows us to be a company that prospers, grows and empowers women to experience healthier lives. None of this would be possible without the talent, skills and aspirations of our employees. Their expertise and dedication to developing and sharing more robust, science-based certainty drives our increasingly global presence, as well as a pipeline that responds to the unmet health and wellness needs of women, families and communities. What powers our growth across Breast & Skeletal Health, Diagnostic Solutions, an
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Snel solliciteren
SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Understanding the specific needs of over 35 countries we operate in, balancing between standardization and local adaptation. * Translating these market requirements into clear supply chain processes. * Managing projects, coordinating with internal teams and external . * Managing distribution processes, designing solutions that meet business and IT needs. * Ensuring smooth communication between business teams and IT departments, especially for market-specific solutions. * Leading Request for Proposals (RFP) processes with external and writing user stories when necessary. Votre profil * Master's degree in Sciences * Minimum of 5 years of experience in Supply Chain, ideally with expertise in distribution networks, supply chain managem
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Barry Callebaut * Lebbeke-Wieze, BE, 9280 * Contract duration unspecified * Full Time - Introduction - At Barry Callebaut, we are on a journey to transform the cocoa and chocolate industry. As the world's leading manufacturer of high-quality chocolate and cocoa products, our actions truly shape the future of our industry. We are a business-to-business company, serving the entire food sector, from the cocoa bean to the finest chocolate product. We are a company with a purpose, we believe in doing well by doing good and reinvesting in the communities we operate. We have a long-standing commitment to sustainability and our goal is to shape a sustainable cocoa and chocolate future. We are headquartered in Zurich, and have more than 12,000 passionate Employees working in more than 40 countries worldwide. We are very proud of who we are and what we do.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - As a Gene Therapy Quality Partner, you will support the Genesis project GMP Readiness program to timely obtain health authorities authorization to manufacture Gene Therapy clinical batches in the new facility pilot plant. * Drive the implementation of the new Gene Therapy facility quality operational procedures into existing QMS (change control, deviation management, release procedures, training, etc). * Support the documented assessment of the GMP & Operations Readiness program progresses according to project key milestones. * Support management of materials & product specifications, execute incoming materials release * Support the consolidation and writing of the Contamination Control Strategy * Drive the 's qualification program
Orion Pharma BVBA * Mechelen * Contract duration unspecified * Full Time - Introduction - At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life. Your Challenge - Reception & administration * Handling incoming calls and mails * Welcoming visitors * Handling medical inquiries and adverse drug reaction reports * Planning business trips * Assist in organizing congresses and events * Support to office team for administration, presentations and reporting * Assist in fleet management * Administrative support to sales team for scientifi
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 - Contracting – Brabant Wallon - Vos responsabilités * Validate the integrity of transferred and transformed data in the new system. * Draft and execute validation protocols (tests, reports, documentation). * Define User Requirement Specifications (URS) and ensure compliance. * Collaborate with IT and business teams to guarantee data accuracy and consistency. * Manage a backlog of dashboards awaiting validation and ensure effective follow-up. * Communicate with various (IT, Business, QA, QC). * Be proactive in coordinating tasks and following up with . Votre profil * Bachelor's degree in Sciences * Proven experience in data validation, preferably in a regulated environment. * Strong proficiency in SQL for executing tests and validating data.
Barry Callebaut * Lebbeke-Wieze, BE, 9280 * Contract duration unspecified * Full Time - Introduction - At Barry Callebaut, we are on a journey to transform the cocoa and chocolate industry. As the world's leading manufacturer of high-quality chocolate and cocoa products, our actions truly shape the future of our industry. We are a business-to-business company, serving the entire food sector, from the cocoa bean to the finest chocolate product. We are a company with a purpose, we believe in doing well by doing good and reinvesting in the communities we operate. We have a long-standing commitment to sustainability and our goal is to shape a sustainable cocoa and chocolate future. We are headquartered in Zurich, and have more than 12,000 passionate Employees working in more than 40 countries worldwide. We are very proud of who we are and what we do.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - Our client is looking for a Documentation & Training Coordinator for a major project aimed at modernizing the artwork management system. This role is crucial to ensure the update and finalization of associated documentation, as well as the coordination of training for . The person hired will work closely with a dynamic . * Coordinate the update of documentation according to the new defined structure. * Support Subject Matter Experts (SMEs) to ensure the timely delivery of documents. * Monitor and manage the documentation schedule. * Plan and organize the user training program (300+ people). * Ensure adherence to the schedule and follow up with in case of delays. * Coordinate the transition period between the old and new systems.
Barry Callebaut * Lebbeke-Wieze, BE, 9280 * Contract duration unspecified * Full Time - Introduction - At Barry Callebaut, we are on a journey to transform the cocoa and chocolate industry. As the world's leading manufacturer of high-quality chocolate and cocoa products, our actions truly shape the future of our industry. We are a business-to-business company, serving the entire food sector, from the cocoa bean to the finest chocolate product. We are a company with a purpose, we believe in doing well by doing good and reinvesting in the communities we operate. We have a long-standing commitment to sustainability and our goal is to shape a sustainable cocoa and chocolate future. We are headquartered in Zurich, and have more than 12,000 passionate Employees working in more than 40 countries worldwide. We are very proud of who we are and what we do.
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Walloon Brabant - Vos responsabilités * Participate to the development of new products and processes * Give directions from early development up to lifecycle management, from particle design up to final product * Work autonomous, well-organized and use your pro-active thinking skills * Be self-reflective on the gathered data * Use your creativity to develop new analytical methods or even develop new technology * Drive team spirit and encourage collaboration * Being a leader in powder characterization by leveraging Materials Science to drive overall Product Development in order to obtain the right drug for every patient * Guide the Product Development by connecting powder /particle insights with manufacturing technologies and overall product performance
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Brabant Wallon – Contracting - Vos responsabilités - 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. * Contribute to project sub-team (DS, DP or analytical) as senior SME representing own area of expertise and actively contributing to the elaboration of project strategy.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Oversee Design & Development activities, from Inputs definition through Design Transfer (including Validation/Verification activities) * Review and approve relevant sections of the device design control documentation and/or Technical Documentation File as required * Review and approve protocols and reports for Verification & Validation studies, technology transfers, stability studies, etc… * Review and approve the company documentation. Ensure Design History File (DHF) is in place * Support Risk Management Activities related to devices. Ensure risk assessments are performed at appropriate stages of development/commercialization and for decision making on issues arising. * Ensure deliverables are issued in accordance with the D&D pl
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
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Jefferson Wells * Braine l'Alleud * Contract duration unspecified * Full Time - Contracting – Brabant-Walloon - Your responsibilities * Development of an in-depth understanding of the process chemistry and process engineering relating to the postholder's projects and an awareness of chemical aspects of other projects within the group. * Execution of preliminary literature surveys leading to the definition of experimental programs. Planning, preparation and implementation of experimental and/or scale-up studies using standard and specialized equipment and techniques (laboratory, kilo-lab & pilot plant). Initiation, monitoring and work-up of reactions as well as isolation and purifications of materials (laboratory, kilo-lab and pilot scale). * Identification and definition of specific analytical tests in order to facilitate effective process development and ensure optim
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Drive and promote a continuous quality and compliance mindset within Clinical Packaging & Logistics Operations, ensuring compliance with cGMP's and the company Quality Management System * Partner with Clinical Supply Compliance Team and management to quality initiatives that develop and maintain a high performing, scalable, and compliant quality system in CPLO. Ensure close interface with QA, CS Compliance and CPLO teams. * Coordinate and/or participate in the implementation of new regulatory standards within CPLO processes. * Represent the interests of the CPLO teams, serve in multidisciplinary Compliance project teams, working closely with other in a cooperative way to ensure project progression
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - Our client is looking for a Procurement Specialist, responsible for procurement operations at a biological production facility for raw materials. This role is crucial in ensuring a smooth supply chain transition from project phase to commercial production. * Manage procurement operations, ensuring timely ordering and delivery of materials. * Process purchase orders and monitor stock levels using SAP (MM module, client-side transactions). * Communicate with planning teams and to guarantee smooth supply chain operations. * Handle supplier negotiations related to delivery schedules and urgent needs. * Address quality investigations in coordination with and internal teams. * Serve as the main point of contact for operational procuremen
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
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Lead and coordinate the laboratory expansion and modernization project. * Manage commissioning and qualification activities for equipment and installations. * Collaborate closely with various internal departments and international . * Ensure compliance of facilities and processes with regulatory standards (GMP Pharma). * Identify technical needs and propose appropriate solutions. * Monitor project progress, manage risks, and maintain regular communication with . Votre profil * Bachelor degree with 5 years of relevant experience or Master's degree with 3 years of relevant experience; degree in science, engineering, or a related field. * Pharma skills (change request, deviation, capa…). * Mastery of laboratory processes and associate
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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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Smals Data Scientist * Brussel * Vast contract, onbepaalde tijd * Thuiswerken mogelijk - Smals realiseert innovatieve ICT-projecten in e-government en e-health voor instellingen uit de sociale zekerheid en de gezondheidszorg. 'ICT for society' is voor Smals meer dan een slogan: alle projecten hebben een positieve maatschappelijke impact. Zo bouwt Smals mee aan het portaal van de sociale zekerheid en het eHealth-platform. Jouw verantwoordelijkheden - Als Data Scientist speel je een belangrijke rol in de ontwikkeling en validatie van onze datagestuurde oplossingen. - Strikte testprotocollen ontwikkelen om nauwkeurigheid van predictieve modellen te valideren. - De prestaties van de algoritmen optimaliseren door de hyperparameters bij te sturen. - Zorgen voor een efficiënte integratie van de modellen in de productieomgeving.