Reistijd
... Min.
Sollicitatie methode
Taal van de job
Vaardigheden
Functiecategorie
Sector
Regio
Gemeente
Ervaringsniveau
Type contract
Voltijds/deeltijds
){kind=logo}
Une expérience professionnelle dans un environnement réglementé (Pharma, Nucléaire, ATEX) est souhaitée.
Connaissance des risques fréquemment rencontrés sur un chantier, et en maitriser les mesures de prévention (travaux en hauteur, consignation, ATEX, manutention lourde, travail en espace confiné, utilisation de produits dangereux, utilisation d'engins et de machines-outils...) en vue de donner des avis éclairé en matière de sécurité
Connaissance des directives techniques comme : Machine, PED, ATEX, levage,…
){kind=logo}
Dit doe je onder andere door het opstellen van een projectplanning en werkschema's voor je collega-inspecteurs(rices) en door deel te nemen aan meetings met de klant waarbij je meedenkt en adviseert aangaande hoog- & laagspanningsinstallaties, ATEX, branddetectie, normen & wetgeving, …
Deze jobs kunnen interessant zijn voor jou
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. * Using a Risk Based Approach, ensure that all Utilities, HVAC & Cleanroom Systems used by the campus and related supporting services are compliant with applicable regulations and guidelines (EMEA, FDA, PIC/S, ICH, best practices as defined by relevant organizations) and the company Corporate Policies & Procedures. * Support the to develop and implement technically robust and compliant Systems allowing to continuously improve their operations. * Responsible for all cGMP aspects related to the Utilities, HVAC & Cleanroom Systems owned by t
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
Partner with QA and CMC Development/DCS colleagues to identify and mitigate Compliance risks, resolve potential regulatory observations. * 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. * Coordinate the development local instructions, liaise with key stakeholders in order to maintain common practices with regards to “issued copy” within development enti
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * S'assurer que les requis GMP soient intégrés dans le design des équipements / systèmes. * Participer au processus de sélection des vendeurs. * Assurer un oversight qualité tout le long de la phase de construction / installation / mise en service. * Développer les procédures permettant leur utilisation et leur maintenance. * Assurer le release avant utilisation GMP. * S'assurer du respect du timing et de la qualité et aider au respect des budgets. * S'assurer que les procédures sont à jour. * S'assurer que la stratégie de training soit définie. * S'assurer de la correcte implémentation tout au long du projet * Définir le scope et les membres (core team et ad-hoc team). * Leader les discussions du groupe de travail pour dérouler le p
){kind=logo}
As an innovative leader, we are looking for an experienced O&M Engineer to join our team and play a key role in optimizing our hydrogen operational services. 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. * Oversee daily operations of our installations (including 24 wind turbines) via a monitoring system, ensuring
){kind=logo}
Our partner is looking for a Qualification & Validation Engineer to join its team. These positions aim to ensure the qualification and validation of production equipment, primarily for solid dosage forms and packaging. * Qualification and validation of production equipment and installations * 5 to 8 years of experience in qualification and validation within the pharmaceutical industry * Cleaning validation within the scope of technology transfers and pharmaceutical development * Participation in process qualification optimization and continuous improvement * Knowledge of GMP regulations and best qualification practices * Strong experience in cleaning validation is hig
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
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
Oversee Design & Development activities, from Inputs definition through Design Transfer (including Validation/Verification activities) Ensure risk assessments are performed at appropriate stages of development/commercialization and for decision making on issues arising. * Preparation and negotiation of Quality Agreements * Facilitate quality improvement activities at vendors and the company systems * Lead/review critical investigations * Work closely with in the Corporate QA teams (especially CM&C Clinical Supply QA, Corporate Compliance and Affiliate Quality Services) and key Technical Operations teams/Affiliate teams to ensure that all QA services for selected critical vendors are provided in an effective and efficient way * Work in accordance with HSE and Corporate
Minimum 3-5 years of experience in Quality Assurance in a regulated pharmaceutical environment or other life science or health-related field. * Experience in manufacturing batch record QA review and deviation QA review is a must. 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 * Experience in pharma is a must (must quickly become autonomous): experience with chemical/pharmaceutical production, development, and/or regulatory requirements, inclu
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
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
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
Our partner is currently looking for a CMC Quality Solutions Specialist. Additionally, the CMC Quality Solutions Specialist will represent the CMC Quality Lead team when assigned to projects and initiatives. * Review and approval of CMC sections linked to regulatory original submissions, renewals or variations during any moment of the lifecycle management of the assigned products as needed * Product Quality Complaint Committee preparation and complaints oversight * Minimum of 3 years working in the pharmaceutical/biologics industry in a quality management position. Operational experience in GMP in Quality, Manufacturing, or Quality Control would be an
Ensure the promotion of awareness of applicable regulatory and quality management system throughout the Braine Bio DS staff. * Develop appropriate tools to collect quality-related risks and ensure escalation as per companies quality management system. * Make connection within companies organization to improve visibility and influence of the team (e.g., quality systems & strategy, internal manufacturing quality, global quality auditing). * Demonstrated experience in quality system / quality compliance. Jefferson Wells * Braine l'Alleud * Contract duration unspecified * Full Time - Contracting – Brabant-Walloon - Your responsibilities * Support network initiatives related to quality and compliance for local implementation; act as connection for global initiatives related to quality and compliance for lo
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
){kind=logo}
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.
Jefferson Wells offers you a permanent contract as with an attractive salary package and will give you access to trainings in technical matters and soft skills. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Focus on large-scale equipment for the facility. * Package owner : Supplier management, equipment final design, execution and qualification, P&ID tracking, electrical schematics, project execution (planning, coordination,….). Votre profil * Master's degree * Minimum 5 years of experience within pharmaceutical companies and working with Engineering offices * Requires project management experience in pharma, knowledge of qualification, and equipment design. * Experience: Preferably in CAPEX projects within a commercial GMP facility. * Good Upstream and Downst
){kind=logo}
Nous recherchons actuellement un(e) : Quality Operations Lead(m/f) En tant que Quality Operations Lead, vous organisez le suivi des activités quotidiennes du département QC. * Manage * Contrat fixe à durée indéterminée * Plein temps - Nous offrons aux sociétés pharmaceutiques une large gamme de services sur mesure dans les domaines variés tels que les affaires réglementaires, la distribution et la promotion de produits pharmaceutiques ainsi que les services logistiques personnalisés. Basé à Manage, nous recherchons des profils talentueux et dynamiques pour compléter nos équipes et nous accompagner dans notre développement. Votre fonction - Dans ce rôle vous rapportez directement au . Garantir le bon déroulement des activités day to day du département * De la vérification qualité des réceptions de prod
They will be responsible for exploring both external supplier solutions and internal potential solutions to enhance our QC processes. * Utilize technical knowledge in automation to identify opportunities for innovative process improvements in microbiology. * Assess current QC microbiology processes and recommend automation solutions. * Knowledge of regulatory requirements related to QC microbiology processes. Jefferson Wells * Wavre * Contrat fixe à durée indéterminée * Plein temps - Walloon Brabant – contracting - Our partner is seeking a highly motivated and experienced Consultant to lead an innovative automation project in the Global Quality Control (QC) area, specifically focusing on microbiology. The ideal candidate will have a strong background in automation, excellent communication skills, and
){kind=logo}
Nous recherchons un Ingénieur Qualité Béton pour notre client. * Optimisation des produits et des coûts : Gérer les recettes béton, sélectionner les matières premières, optimiser les coûts des produits et du laboratoire. * Idéalement titulaire du cours "Technologie avancée du béton" du Groupement Belge du Béton (GBB). * Expérience de 5 ans minimum dans le secteur du béton ou en gestion de la qualité des produits. * Innovation et support technique : Développer des solutions durables (réduction du CO2, recyclage), accompagner les clients et la force de vente avec des conseils techniques, contribuer aux projets R&D et gérer les réclamations clients. * Ma