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2 resultaten voor Chemisch laborant in Waals Brabant binnen een straal van 30 km
Jefferson Wells * RIXENSART * Contrat fixe à durée indéterminée * Plein temps - Brabant Wallon - Contracting - Vos responsabilités * Responsable d'organiser et exécuter des expériences de laboratoire upstream (culture cellulaire en adhérence in vitro) définies avec le en démontrant une expertise autant dans l'exécution que dans l'interprétation des résultats obtenus. * Faire preuve de séniorité en termes de résolution de problème, de polyvalence, d'organisation du travail et d'esprit critique. * Travailler principalement en laboratoire afin de pouvoir reproduire à petite échelle les étapes d'upstream de production de nos vaccins (culture cellulaire et tests in process associés), en participant aux tâches quotidiennes et en respectant les consignes de sécurité. * Ecriture des checklists de laboratoire électroniques et des rapports décrivant les objectifs et les résulta
Jefferson Wells * RIXENSART * Contrat fixe à durée indéterminée * Plein temps - Brabant Wallon - Contracting - Vos responsabilités * Responsable de planifier, et des méthodes analytiques sur base de différentes familles de technologie (principalement tests d'infectivité sur cultures cellulaires en adhérence in vitro) en démontrant une expertise autant dans la planification, l'exécution que dans l'interprétation des résultats obtenus. En cela, il/elle doit faire preuve de séniorité en termes d'expertise technique analytique, de résolution de problème, de polyvalence, d'organisation du travail et d'esprit critique. * Travailler principalement en laboratoire en réalisant des expériences analytiques, en participant aux tâches quotidiennes et en respectant les consignes de sécurité. * Ecriture des protocoles, checklists de laboratoire et des rapports décrivant la méthodolo
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Afin de rejoindre le département de Chimie de notre laboratoire de SGS Lab Simon à Wavre, nous sommes actuellement à la recherche d'un(e) « analyste en CHEMISTRY - PHYSICS » * Formation de niveau A1 (bachelier) en chimie analytique * Enregistre promptement, précisément et intégralement les données nécessaires à la traçabilité des opérations effectuées conformément aux procédures en vigueur (échantillons, réactifs, appareillages, initiales, dates) ; * Signale immédiatement tout résultat hors spécification au Team Leader conformément à la procédure en vigueur ; * Signale au plus vite au Team Leader tout besoin en matériel et réactifs ; * Respecte les procédures mises en vigueur, signale les écarts au Team Leader ; * Exp
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Nous sommes actuellement à la recherche d'un(e) Analyste en Chimie pour rejoindre nos laboratoires SGS Lab Simon et SGS LCA. SGS Group Belgium * Wavre * Contrat fixe à durée indéterminée * Plein temps - Description de l'entreprise - SGS est une société internationale d'inspection, de vérification, de testing et de certification. Description du poste * Effectue les essais de conformité sur les matières premières ou produits finis. * Enregistre promptement, précisément et intégralement les données nécessaires à la traçabilité des opérations effectuées conformément aux procédures en vigueur (échantillons, réactifs, appareillages, initiales, dates). * Signale immédiatement tout résultat hors spécification au superviseur de laboratoire conformément à la procédure en vigueur. * Signale au plus vite au Team Leader tout besoin en matériel et réactifs. * Signa
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-Walloon - We are looking for a PCR expert to join our team ! Vos responsabilités * PCR method development, qualification, non-GLP sample testing and reporting, to deliver high quality data to advance UCB's gene therapy portfolio * Work within the to develop and optimize processes related to experimntal design, sample testing, and report generation. * There may be opportunities to support the method development and sample testing for other bioanalytical methods including cell-based immunogenicity assays - Votre profil * At least a BSc, preference for an MSc in a relevant biological discipline with more than 3 years of experience in bioanalysis. * Demonstrated advanced technical understanding of PCR assay development and optimization, experience with qPCR and digi
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
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
Assurer la coordination de la validation des projets majeurs de TRD GMP en Drug Substance et Drug Product. * Assurer l'approche 'state of art' de la Validations du plan de validation (= stratégie de validation) jusqu'au Validation Summary Report, incluant : Ecriture, la revue et approbation de document de validation tels que les Risk Assessments, les protocoles IQ/OQ/PQ, les rapports IQ/OQ/PQ … * Expertise en validation IQ/OQ/PQ et GMP, solides connaissances en organisation matricielle et en gestion de projet. * Connaissance en validation de produit injectable. Jefferson Wells * RIXENSART * Contrat fixe à durée indéterminée * Plein temps - Consultance – Brabant Wallon - Vos responsabilités * Coordination de l'exécution des protocoles.
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Active member of Lab Quality meetings: act as strong and project. * Be responsible for metrology aspect: Ensure mapping and reports delivered by the External vendors are compliant with the specificities defined by the Lab. * Assures accurate collection and processing of biological specimens to assure quality of analytical data. * Integrate and monitor quality indicators (key performance indicator = KPI), handle non-conformities and claims as well as corrective and preventive actions. Jefferson Wells * Brussels * Contract duration unspecified * Full Time - Brussels – contracting - Your responsibilities * Lead Equipment management process * Be the SME on that process for the entire unit * Train the from equipment purchase to equipment installed. * Ensure at least 1 internal Audit/year.
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
Representing the non-clinical safety team in cross-functional meetings * Good knowledge about non-clinical safety evaluation of starting materials, synthesis intermediates and impurities, degradation products, leachables and extractables and associated guidelines. Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Walloon – Brabant - Your responsibilities * Writing and monitoring risk assessments for impurities (eg, justification of specifications, elemental impurities risk assessments, extractables and leachables, degradation products, ICH M7-compliant evaluations, etc.) * Planning, coordinating and monitoring the conduct of toxicology studies at contract research organizations in line with project timelines and budget * Performing and monitoring toxicological risk assessments for various he
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting - Brabant-Walloon - Vos responsabilités * Rédiger et mettre à jour les documents liés à la CCS * Organiser proactivement des réunions afin de collecter les informations auprès des * différents stakeholders (Production, Validation, Maintenance, Qualité, QC, MSAT…) * Développer un visuel afin de faire ressortir les éléments clés de la CCS (draft existant). * Ces documents doivent être finalisés pour l'inspection AFMPS de Juin. * Être en ordre de formation pour les activités dans le scope * Remonter tout problème significatif qui pourrait présenter un risque (qualité, coût, timing…). * Communiquer avec l'ensemble des pour assurer un mode de travail * coopératif. * Supporter les activités requises par le projet. Votre profil * Master * Bonnes connaissances des requis règlemen
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Research Scientist in Histology and Image Analysis for Neurodegenerative Diseases
Research Scientist in Histology and Image Analysis for Neurodegenerative Diseases
Jefferson Wells
Braine-l'Alleud
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting - Brabant-Walloon - Vos responsabilités * Performing immunohistochemistry on brain sections, high-throughput image acquisitions using different microscopy instruments, and image analyses using advanced technologies such as artificial intelligence. * Regular interaction with and from different departments within the company, as well as with external organizations, to organize studies and ensure their completion. * Interpreting data and reporting results in an organized and timely manner. * Performing other duties as required and assigned. * Knowledge in neuroscience and neuroanatomy is preferred (rodent, monkey, or human brain). * Expertise in immunohistochemistry (fluorescent, colorimetric) and general knowledge in the field of histology with at least 2 years of experienc
Active member of Lab Quality meetings: act as strong and project. * Be responsible for metrology aspect: Ensure mapping and reports delivered by the External vendors are compliant with the specificities defined by the Lab. * Assures accurate collection and processing of biological specimens to assure quality of analytical data. * Integrate and monitor quality indicators (key performance indicator = KPI), handle non-conformities and claims as well as corrective and preventive actions. Jefferson Wells * Brussels * Contract duration unspecified * Full Time - Brussels – contracting - Your responsibilities * Lead Equipment management process * Be the SME on that process for the entire unit * Train the from equipment purchase to equipment installed. * Ensure at least 1 internal Audit/year.
Expertise in lab relocation is a plus - 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
Ability to participate to process development as scientist in specific area of expertise as process characterization, optimization, understanding, industrialization and investigation QbD development of the different compounds in development. * 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. * Identification and definition of specific analytical tests in order to facilitate effective process development and ensure optimum product quality. * Participation in the transfer of chemical processes from laboratory to kilo-lab, pilot plant and/or production, under the direction of Science lead. * Knowledge in
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
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To support the growth of our European Technology Center (ETC) in Brussels, we are looking for several Research Technicians in different groups. The Exxonmobil Research Technicians at ETC in Machelen are giving support to their related business units. The office building in Brussels (Machelen) houses ExxonMobil's regional headquarters for Europe, Africa and the Middle East (EMEA) and the European Technology Centre (ETC) for research and development. In ETC we strive to develop and maintain state-of-the-art capabilities to advance research in support for businesses throughout ExxonMobil. Research topics span from the discovery of novel catalytic material for new or more efficient production processes, to the development of next generation packaging solu
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 * Be one of the QA representatives in case of external audits regarding specific domain of knowledge (Master Data, purchasing, vendors management, warehouse, ... ) * In response to business requirements, identify, treat and communicate to QA and BTO management the possible issues of non-cGMP/21 CFR 820 compliance within Quality Management System and provide cGMP and QA expertise, interpretation and direction in order to create a framework of operational excellence enabling implementation of continuous improvement (e.g.: technical changes). * Train the company personnel regarding cGMP/21 CR 820 and Level of Quality requirements related to supply chain, purchasing, warehouse, operations, cold chain and SAP aspects.
SME Support: Provide technical expertise as needed in engineering and processes, especially in IT, data security, and automation. Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Walloon Brabant - Your responsibilities * Project Management: Coordinate a portfolio of projects (mainly in secondary packaging and medical devices), ensuring proper management of schedules and critical milestones. * Inter-project Coordination: Link technical teams, production, and experts (IT, automation) across different departments. * IT/Automation Project Oversight: Manage projects related to Data Integrity, IT security, and the automation of manufacturing facilities. Your profile * Project Management Skills (tools like MS Project). * Technical Knowledge in engineering, particularly in pharmaceutical production (secondary packa
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Dans le cadre du renforcement des équipes de production, notre partenaire est à la recherche d'un(e) Technicien(ne) de production pour intégrer le site de Nivelles. Vous serez en charge de l'exploitation et de la maintenance des lignes de production, en veillant à garantir la qualité, la sécurité et la performance de la production dans le respect des normes en vigueur. * Vous assurez le bon fonctionnement des lignes de production en suivant les procédures opérationnelles établies. * Vous assurez un reporting régulier de votre activité auprès du responsable de production (temps d'arrêt
Manage the research outsourcing lifecycle under supervision, including service provider assessment, contract negotiation (e.g., Confidentiality Agreements, Services Agreements, Material Transfer Agreements, Consultancy Agreements), performance monitoring, contract amendments, budget monitoring, and study closeout. * Support the management of outsourced activities and collaborations within the internal departments (including elements of early development), including interactions and negotiations with external partners such as Contract Research Organisations, consultants, and non-commercial partners. * Optimize the outsourcing process in close collaboration with key departments. Adopt the Contract Lifecycle Management system for creating template-driven outsourced activities, including contract archivin
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. * Design DP processes for sterile injectable drug products in liquid or lyophilized powder form, in vials, pre-filled syringes or as combination products). * Define the investigational medicine product preparation process in clinical trials. * Provide support to process performance qualification/validation Ensure products are manufactured in accordance with the company quality system, cGMP and latest regulatory requi
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