Opties voor telewerken
Reistijd
... Min.
Sollicitatie methode
Taal van de job
Vaardigheden
Functiecategorie
Sector
Regio
Gemeente
Ervaringsniveau
Type contract
Voltijds/deeltijds
Voltijds
23
24 resultaten voor Kwaliteitsborging in Nijvel binnen een straal van 30 km
){kind=logo}
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Promote Quality and Operational Excellence and cultivate “Quality Culture”, “Compliance Awareness”, “Continuous Improvement Attitude” & “Accountability Culture” across the UCB teams. * Drive Quality Leadership on Quality & Compliance Strategy and interact with other functional areas to effectively communicate system & process requirements. * Maintaining and continuously improving the Quality Management System and related processes. * Ensuring continued compliance of the QMS to applicable regulations and guidelines, the company Corporate Policies & Procedures, objectives, plans and projects. * Using a Risk Based Approach, ensure that all Utilities, HVAC & Cleanroom Systems used by the campus and related supporting services are compl
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * S'assurer du respect cGMP. * 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 * Participer activement à la préparation des lots de process performance qualification (PPQ). * 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.). * Expérience dans un environnement GMP. * Bonnes connaissances des systèmes qualité (QMS) : Déviations, Change Control, CAPA. * Bilingue en Français et Anglais. Notre offre
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 * 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
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Perform mapping of current situation of qualification/validation status in CMC Dev * Evaluate risk and define remediation plan with system owner * Complete and maintain tracker DT with prioritization * Project Management support for physical assets topics * Drive meetings to support Project * Update documents (sops, process, assessment, slides …) identified in project * Good knowledge qualification and validation process, IT compliance, GMP knowledge, data Integrity principles * Drive remediation plan, coordinate and finalize actions * Drive dashboard for for Dev entities * Interaction transversal entities (IT, Manufacturing, biological, chemical, QA, outsourcing Lead …) * On site assignment - Votre profil * Master/Bachelor: Biolog
){kind=logo}
Institut National des Radio Elements * Fleurus * Contrat fixe à durée indéterminée * Plein temps - Introduction - Situées à Fleurus, avec plus de 280 collaborateurs, l'Institut National des Radioéléments (IRE) et sa filiale IRE ELiT sont des entreprises industrielles renommées et innovantes. L'IRE est un leader mondial dans la production de radio-isotopes à destination de la santé publique, principalement dans les domaines du diagnostic et de la thérapie. L'IRE est également active dans le domaine de la surveillance de l'environnement et de la protection de la santé au travers de prestations de services. Sa filiale, IRE ELIT, est quant à elle active dans la production de médicaments radiopharmaceutiques. Plus concrètement, ces entreprises contribuent à sauver des millions de vies dans le monde chaque année.
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * 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 to build the end to end “issued copy process' for DEV/DSC entities. * Act as Reconciler by checking the correct completion of the “issued Copy” pro
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 * 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.
){kind=logo}
Smals Facility Officer * 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 Facility Officer verzeker je de administratieve, contractuele en budgettaire opvolging van de projecten. Je werkt daarbij nauw samen met de , overheden, interne en externe klanten, techniekers en de dienstverantwoordelijke. • Het onderhoud, de technische controle van de gebouwen en informaticacentra opvolgen. • Elektriciteitsdistributie- en HVAC-projecten ontwerpen, dimensioneren en opvolgen.
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 * Wavre * Contrat fixe à durée indéterminée * Plein temps - Brabant-Walloon - Contracting - Vos responsabilités * To take part in the establishment, the implementation, the follow-up and the maintenance of the continuous validation plan (CVP) * To define the validation strategies through the change control process (change control & MO notification) - Remark : No signature as task approver/stakeholders. * To write and implement some validation documentation (VP, VSR) * To review and approve specific qualification and validation documentation (IQ, OQ, PQ, Risk Assessment, Periodic validation review - Remark : No signature as final approver for equipments with high criticality. * To ensure the correct application of the validation quality systems on the field and to define improvement plan as required
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 * 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
){kind=logo}
Sander Brussels * Brussel * Contract duration specified * Full Time - Drive quality and innovation with your test automation skills in a dynamic tech team. Join a company at the forefront of secure and high-tech solutions, where innovation and quality go hand in hand. As a Test Automation Engineer, you will be part of a collaborative and forward-thinking environment, working on impactful projects that shape industries. Your role will be crucial in designing, developing, and maintaining automated testing frameworks, ensuring that our software solutions meet the highest standards of reliability and performance. If you thrive in a dynamic setting where technology, security, and efficiency are key, this is the perfect opportunity for you! Responsibilities * Develop and implement automated test scripts for software applications. * Collaborate with and to enhance testing st
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - Notre client est à la recherche d'un Project Manager Engineering Capex à consonnance technique pour driver un de leurs projets clefs. Le projet concerne la distribution centralisée de solvant dans le bâtiment upstream. Il souhaite retirer les fûts de solvant de la zone de production et centraliser leur alimentation via des cuves tampons, et de manière automatisée. * Comprendre et driver les aspects techniques de ce projet (et leader une équipe composée de chimistes, process engineers, automation engineer, electrical engineer, EHS, QA technique…) * Mettre à jour le budget et le forecast du projet * Suivre et leader le planning du projet * Leader les achats (la négociation se faisant via le procurement manager),
){kind=logo}
Barry Callebaut * Halle * 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.
){kind=logo}
Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Brabant Walloon – contracting - Our partner is looking for a Qualification & Validation Engineer to join its team. This international company is well-known for its pharmaceuticals. These positions aim to ensure the qualification and validation of production equipment, primarily for solid dosage forms and packaging. Your responsibilities * Qualification and validation of production equipment and installations * Cleaning validation within the scope of technology transfers and pharmaceutical development * Participation in process qualification optimization and continuous improvement * Support for various expansion and production capacity optimization projects * Interaction with production, maintenance, and quality assurance teams - Your profile
){kind=logo}
Brabant wallon * Contrat fixe à durée indéterminée * Plein temps - Votre nouvelle société - Notre client est une société internationale active dans le monde entier et spécialisée dans la gestion et la distribution de produits pétroliers et chimiques. Afin de renforcer son équipe Supply Chain, nous sommes à la recherche d'un Product Quality Specialist. Vos responsabilités - Votre nouveau rôle * Gérer la qualité des produits, analyser et déterminer les plans de mélange. * Maintenir la base de données des produits et participer aux audits des terminaux et des laboratoires. * Soutenir le dans l'investigation des plaintes relatives à la qualité des produits, la non-conformité des produits, la planification des audits client. * Soutenir la chaîne d'approvisionnement avec le calcul des recettes pour les mélanges en ligne.
){kind=logo}
Indien nodig kan hij ook projectspecifieke plannen voor kwaliteitsborging opstellen.
Mission Masala & Bombay BBQ * Brussel * Contract duration unspecified * Full Time - Your tasks - Operate across 2 locations in Brussels (Bombay BBQ & Karma kitchen) and support the teams with the daily running of the kitchens. * Operate all stations with ease and efficiency and handle the tasks typical of a kitchen, including preparing, cooking, cleaning, training, and quality assurance. * Tasks include operating a Tandoor, BBQ, fryer, wok, and the pass: - Preparing doughs & breads - Applying marinations & preparing skewers * Frying and finishing items - Strong MEP skills to set up for the Wok station - Able to multitask and maintain strong communication at the pass * Stepping in to relieve all staff during their annual leave. * Remain attentive to all parts of the culinary process to ensure that customers receive the highest-quality food.
ING South West Europe: Change & Acceptance Management - Qualitas Software
ING South West Europe: Change & Acceptance Management - Qualitas Software
Qualitas Software BV
Beukenlaan 53a Tervuren
Qualitas Software BV * Beukenlaan 53a Tervuren * Contract duration unspecified * Full Time - Your tasks • Change Management (appl & infra) & project co-ordination (V-life cycle), ITIL, Sox 404 (Sarbanes Oxley 404) compliant, GPL Prince 2. Team coaching • Chairman of Change Management Committee (CMC), Change Implementation Board preparation (CAB), Governance process. Program / large projects in scope: Business Intelligence (Data warehouse), Risks, Financial Architecture Reengineering, HR and Web (Application Project Management (APM) & Key Project Management (KPM)) • Program/Projects Change Management • Bring new business-applications (appl & infra), (project) • Bring new releases of business-applications (maintenance) • Bring small enhancements (fixes, incidents, problems) • Define, plan, monitor and coordinate IT acceptance test activities (design, preparation, execut
Council of the European Union Consilium: Quality Management - Qualitas Software
Council of the European Union Consilium: Quality Management - Qualitas Software
Qualitas Software BV
Beukenlaan 53a Tervuren
Qualitas Software BV * Beukenlaan 53a Tervuren * Contract duration unspecified * Full Time - Your tasks - Test Management (umbrella of very sensitive core business applications, BREXIT, Single Resolution Mechanism, Delegates Portal (40.000 users), Delegated Acts, Restrictive Measures, Prepare next Presidency, …), internal and outsourced developments (ALFRESCO & AZURE Cloud). Internet & Intranet applications, front-end, and back-end. • Managing (lead/coach) Agile testing team and testing campaigns • Agile/DevOps Continuous delivery – Continuous testing (Scrum/Kaban) • TMMi improvements (L1 => L3) • Restricted military domain. Initially, more Hot Fixes than releases, after the implementation of Quality Processes, we significantly reduced the % of Hot Fixes close to 0%. Proven ability to deliver against the deadline and budget. PBR methodology (Plan/Build/Run) based on P
SERCO BELGIUM Nv * OUDERGEM * Not available - Job Introduction - In Europe, we work closely with our customers to deliver custom-made and specialized services across International Organizations, Space, Immigration, and Defence. We look forward to meeting you! Main Responsibilities - Technical Operations & Maintenance * Oversee the technical aspects of hard FM services, including building maintenance, HVAC, electrical, plumbing, fire safety, and security systems. * Consult on preventive and corrective maintenance programs to optimize facility uptime and longevity. * Implement energy efficiency and sustainability initiatives to enhance operational resilience. * Manage the installation and commissioning of new equipment, ensuring compliance with operational requirements. * Troubleshoot and resolve complex technical issues related to construction and facility management.
Deze jobs kunnen interessant zijn voor jou
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