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20 resultaten voor Wetenschappen in Waals Brabant 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
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
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Be the central QA point of contact for the organization for investigations / deviations / out-of-specifications / audit observations associated with the assigned vendors. Perform the QA review of deviation notifications, retrieve and collect supportive information from involved stakeholders (the company Vendor Team, GQL, ILA, ALO, Business) to allow assessment. * Manage the key performance indicators (metrics) for key operational QA activities and services associated with the vendors in the defined described tracking tools ( QA KPI tracker, Spider Impact) and track the 's performance * Ensure all Quality agreements are in place and take ownership of agreements for the vendors.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Execution of routine analytical experiments and method development activities under supervision. * Follow established procedures and protocols. * Collaborate with in routine tasks. * Seek guidance for troubleshooting and problem-solving. * Decision-making, primarily under supervision. * Follows standard protocols under supervision. Identifies issues with guidance. * Support and assist in project/operation planning, data analysis, and coordination. * Follows project/operational plans and guidelines. * Assists in project tasks under supervision. * Collaborates with and provides status updates. * Sample management (availability in lab, shipment and reception). * Day to day lab experiment/resources planning and equipment booking in GT
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
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.
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.
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 - 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 – 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 - 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 - 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 - 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.
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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 * 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
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - As a Digitalization Officer, you will assist in the implementation of an Electronic Batch Record (EBR) system for the visual inspection process within a plant. This project aims to transition from a paper-based documentation system to a fully digitalized process, ensuring enhanced traceability and efficiency. * Participate in the testing phase (Dry Run) of the EBR system by validating different sequences and ensuring compliance with expected outcomes. * Act as the Representative, bridging communication between the production floor, engineering, IT, and qualification teams. * Support the implementation of digital tools in the production environment. * Conduct technical testing and verification to ensure process efficiency and system
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 . * Provide support during regulatory inspections, and quality improveme
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Brabant Wallon – Contracting - Vos responsabilités - Responsable de la gestion du laboratoire, incluant principalement la gestion et maintenance des équipements, la gestion des commandes, la supervision de la biosécurité, et la gestion des stocks, au sein de l'équipe de notre partenaire actif dans l'industrie pharmaceutique. L'exécution d'expérimentations spécifiques de laboratoire pourra également être requise. * Gestion des équipements de laboratoire (interventions, planning de maintenance et des nettoyages/décontaminations). * Gestion des stocks (consommables, milieux, solvants, …). * Remise/réception des colis. * Gestion de commandes. * Gestion de la biosécurité. * Réalisation de différentes manipulations de laboratoire (appui technique) en fonction des applications du groupe, pr
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Ensuring that operations related to the packaging of finished pharmaceutical products comply with national and/or international regulations and guidelines (GMP), as well as the company quality policies * Ensuring that registered finished products are produced and supplied to markets in accordance with the company quality standards * Proactively assisting operations in identifying, developing, and implementing quality improvements and operational excellence in response to business requirements, technical changes, and regulatory requirements * Monitoring of quality deviations, temporary and permanent change control, CAPA * Support for market complaint investigations with responsible pharmacists
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Assisting in drawing up, review and approval of procedures and instructions related to these activities * Being one of the QA representatives for those activities and departments on the company site in case of alignment and level of quality related issues * Treating alignment and level of quality related issues and follow up on the related corrective and preventive actions (via deviations handling, follow up of change control, initiation of investigation, follow up of complaints) * Performing continuous GAP analysis between new expectations and Quality Management System documentation and between the company documentation and actual practice (update Risk Register regularly)
We hebben je zoekopdracht uitgebreid met 3 vacatures buiten de geselecteerde regio
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MacroArray Diagnostics GmbH * Netherlands, Belgium * Vast contract, onbepaalde tijd * Voltijds - Introduction - We have revolutionized allergy diagnostics and have been operating successfully in more than 70 countries for over 5 years with our diagnostic products and patented technologies. Our products help clarifying allergies in a single step – for humans and animals alike. Allergies are diagnosed in a highly specific manner so that patients receive help by their in no time. We increase quality of life, enable personalized treatment, advance research and relieve our health system. We need you for * Managing key accounts and acting as a point of contact for clients * Representing MADx at conferences * Organizing client meetings to discuss their requirements * Timely resolving problems and handling complaints
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Diploma: Je beschikt over een Master in de Industriële Wetenschappen - Elektromechanica.
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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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Support the increase in laboratory capacity with a team of nearly 50 people, including analysts and specialists. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Cross-Functional Coordination: Work with (TL) to manage deviations, investigations, and priorities. Ensure smooth communication with different teams, especially during urgent situations. * Sample Management: Track samples using tools like LIMS, coordinate their reception, testing, and release, while ensuring compliance with client deadlines. * Deviations and Investigations: Manage deviations, root cause analyses, investigations, and changes related to processes. Precision in managing these tasks is crucial. * Documentation: Manage documentation related to validations, analyses, and regulatory authority r
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