8 resultaten voor Manager Outsourcing in Ittre binnen een straal van 30 km

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Voor de uitbouw van een 2de pijler binnen ons Outsourcing departement zijn we op zoek naar een 2de operations manager. JIJ komt terecht in ons Outsourcing departement waar we gespecialiseerd zijn in het opvolgen van debiteuren voor en in naam van onze klanten. Als people manager ga je de werknemers motiveren en enthousiasmeren, maar je staat ook in voor het naleven van afspraken door als een goede leider te fungeren; Zoals het een goede people manager betaamt, ga je “lead by example” hanteren. Je bent een communicatieve en enthousiaste motivator en je kan met verschillende partijen overweg (jouw manager, teamleden, coaches, klanten en debiteuren);
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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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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
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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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In a context of strong business growth, the Prospector Wind Flanders will reinforce the prospecting team of Virya's Energy Portfolio of wind projects in Flanders, both in agricultural and business zones. Eoly Energy * Braine l'Alleud * Vast contract, onbepaalde tijd * Thuiswerken mogelijk - Jouw verantwoordelijkheden - Company profile - As part of Virya Energy's integrated approach to sustainable energy, our Grid Solutions division—formerly known as Eoly Energy—specializes in developing utility-scale renewable energy projects across multiple markets. We focus on wind farms and solar installations that feed into the energy grid, complementing the commercial and industrial solutions handled by our C&I business line. At Grid Solutions, we develop renewable energy projects from initial concept through construction and into operations.
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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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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. We will be your career partner for each step along the way. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * 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 consolid
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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
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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
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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 - Ensure adequate documentation processes and systems are available and followed for development projects (SOPs / Protocols / Report review…) * Be partner with other departments to identify, mitigate and subsequently resolve complianc
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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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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
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As an Analytical DevelopmentDocument 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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Smals Data Architect Als Data Architect speel je een centrale rol in het ontwerp en de ontwikkeling van het platform voor gegevensanalyse. • Je definieert de architectuur van de verschillende functionele componenten van het platform: integratieprocessen, datakwaliteit en -validatie, data lake, data warehouses, secure processing environment, datacatalogus, advanced analytics & AI, enz. • Je bent verantwoordelijk voor de data-architectuur en de technische architectuur van het analytische dataplatform. • Je bent verantwoordelijk voor het definiëren van de conceptuele modellering van de data. • Je definieert de processen voor master data en repository management. Je werkt samen met de projectteams (, , , BI-ontwikkelaars, data-architecten
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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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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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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. * 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 * Consult and guide the teams in establishment of controls to mitigate compliance risk; * Assist management in the coordination/management of training plans & matrix and ensure
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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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Wat is het gemiddelde salaris voor Manager Outsourcing in Ittre?

Gemiddeld salaris per jaar
63.700 €

Het salaris gemiddelde voor een Manager Outsourcing in Ittre is 63.700 €. De salarissen van Manager Outsourcing in Ittre variëren van 53.000 € tot 72.900 €.