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4 resultaten voor Bedrijfseigenaar Es in Waals Brabant binnen een straal van 30 km

We hebben je zoekopdracht uitgebreid met 4 gelijkaardige vacatures.

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
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Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Brabant-Walloon - Your responsibilities * Monitor the progress of plans and projects, GQA performance, and compliance through * meaningful KPIs. This will boost operational efficiency and agility. Ensure and track appropriate * data entry performance of audit reports and CAPAs in the Veeva audit system. * Enable insights for the company through data collection, entry, and analysis in the audit * management tool (e.g., trending, KPIs, etc.). * Curate data, including quality checks of audit management tool as needed, for * KPIs/metrics on performance and information on trending. * Ensure maintenance and improvement of quality of critical data within the Quality * Management System (includes data entry of audit related information and data * monitoring).
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Snel solliciteren
Clean Power * Mont-saint-Guibert * Contrat fixe à durée indéterminée * Plein temps - Qui sommes-nous? Clean Power est un acteur majeur dans le secteur du nettoyage, actif sur l'ensemble du territoire belge. Reconnue pour son expertise, son engagement envers la qualité et son approche durable, notre entreprise, en pleine expansion, compte aujourd'hui plus de 170 collaborateurs passionnés. Avec des sièges stratégiquement situés à Mont-Saint-Guibert, Mons, Liège et Zellik, nous avons a coeur de répondre efficacement aux besoins de nos clients à travers toute la Belgique. Aujourd'hui, notre équipe se renforce. Nous sommes à la recherche d'un(e) HR Business Partner prêt(e) pour la prochaine étape de sa carrière. Rejoindre Clean Power, c'est intégrer une entreprise dynamique et ambitieuse, où votre implication fera vraiment la différence.
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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
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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
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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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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
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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
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Be the process data owner for Source QMS (Veeva Source Quality QMS). * Responsibility and accountability to maintain and enhancing transversal cooperation between Business process Owners, Digital industrialization team, IT and/or Vendor. * Provide stewardship and functional management to the implementation of strategies for all the company's GxP and non-GxP QA processes. (Veeva Source Quality QMS, …) * Proactively seek for continuous improvement and develop and share best practices solutions and processes in terms of organization, positive attitude, harmonized work style and customer focus * Excellent ability to analyze information, take initiative and strive for lean processes, efficient and effective training and thus, enhance quality, performance, and compliance. *
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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 . * Coordinate the update of documentation according to the new defined structure. * Monitor and manage the documentation schedule. * Experience in documentation coordination for large projects. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - The person hired will work closely with a dynamic . * Support Subject Matter Experts (SMEs) to ensure the timely delivery of documents. * Plan and organize the user training p
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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.
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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
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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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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. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - 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 effi
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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
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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.
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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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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
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Work collaboratively as part of a wider team and when required deputise for the of Bio MSAT Quality and other Bio MSAT Quality Leads * Process industrialization and Technical transfers within commercial manufacturing facilities * Build, establish and develop a governance model and process for Quality oversight of Internal and External MSAT for Bio Drug Substance and Drug Products which fosters continuous quality process improvement, optimized resource utilization and key indicator based performance monitoring * Promote quality best practices throughout the External & Clinical Supply Quality team and where possible business stakeholders. * Knowledge in multiple areas of Biopharma incl manufacturing and analytical testing, including the
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Translating these market requirements into clear supply chain processes. * Managing distribution processes, designing solutions that meet business and IT needs. * Minimum of 5 years of experience in Supply Chain, ideally with expertise in distribution networks, supply chain management, and customer service management. * Experience in Supply Chain Planning or Logistics role within pharma or food industry. * 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. Jefferson Wells * Braine l'Alle
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Snel solliciteren
Notre client, une société belge leader mondial dans son secteur d'activité et spécialisée dans la fabrication de machines lourdes, recherche un responsable documentation technique/rédacteur de manuel de maintenance. Vous êtes rigoureux(se) et passionné(e) par la documentation technique ? * Intégration des plans électriques et des listes de composants afin de fournir une documentation complète au client. * Contact avec des externes pour la traduction des manuels en plusieurs langues. * Suivi des évolutions des outils de documentation (IXIACCMS, AI, etc.). * Contrôle et suivi de la machine en atelier pour compléter le dossier de maintenance (relevé des numéros de série, mise à jour des procédures de maintenance en fonction des pratiques évolutives…). * Assistance au service après-vente en recherchant des historiques de machines pour proposer des équivalences. * Braine l
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Act as substitute for other Vendor Quality Leads in times of absenteeism (e.g. vacation, illness) * Transfer/Knowledge transfer, commercial (key raw materials to distribution), product improvements to phase out for the assigned vendors * Ensure all Quality agreements are in place and take ownership of agreements for the vendors. Maintain Quality Agreement with the vendors up to date and perform periodic reviews and update of the agreement in close collaboration with the product GQLs and the vendors. * Ensure the Product Quality Reviews (PQR) are completed by the vendors in a timely manner and as needed and are reviewed within the requested time period. * Participate as QA representati
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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
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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
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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
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Wat is het gemiddelde salaris voor Bedrijfseigenaar Es in Waals Brabant?

Gemiddeld salaris per jaar
51.400 €

Het salaris gemiddelde voor een Bedrijfseigenaar Es in Waals Brabant is 51.400 €. De salarissen van Bedrijfseigenaar Es in Waals Brabant variëren van 42.100 € tot 60.000 €.