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7 resultaten voor ATEX in Steenokkerzeel binnen een straal van 30 km
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Une expérience professionnelle dans un environnement réglementé (Pharma, Nucléaire, ATEX) est souhaitée.
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ATEX
Connaissance des directives techniques comme : Machine, PED, ATEX, levage,…
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
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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, …
ATEX
ATEX
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In the spirit of continued growth, we are currently looking for a Head Clinical Project Management. As Head Clinical Project Management (HCPM) you will provide leadership to the team of Clinical Project Managers (CPM) and ensure the allocation of the appropriate CPM resource to the projects. As HCPM, you may assume the responsibilities of a Project Manager in the management of clinical research projects. * Line management: managing and coaching the clinical project management team, providing them with support, advice and assistance, evaluating their 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
Our partner is looking for a Data Reviewer to join its teams. * Perform data review in support of product characterization, release and stability for an extended series of techniques: chromatography, dissolution, karl fisher, particle size, UV, IR, NIR, titration etc - Jefferson Wells * Mechelen * Contrat fixe à durée indéterminée * Plein temps - Contracting - This international company is well known for its pharmaceutical products. Vos responsabilités - Your responsibilities? * Ensure compliance with all relevant regulatory regulations, analytical methods and specifications, GMP and safety. * Scientific evaluation of generated results - Votre profil - Let's talk about you! * You hold a master's degree in science or bachelor with relevant experience * Good knowledge and practical experience with any analytical technique is an asset *
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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
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
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
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
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
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
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
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SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.
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The Global Director Business Development (GBDM) provides leadership and coaching to the Business Development Managers and is responsible for the management of all business development activities of SGS Clinical Research, identifying and exploring strategic business development opportunities to maximize organization growth. We currently have a unique opportunity for a Global Director Business Development for Clinical Research * be accountable for the target realization of the sales and business development activities f
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
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
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
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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Terminal Manager - Sleutelrol Bruisende Multinational
Terminal Manager - Sleutelrol Bruisende Multinational
GS Recruitment BV
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Min 7 jaar relevante werkervaring als terminal manager, operations manager of een gelijkaardige functie, bij voorkeur in de logistiek of een 'terminal'-omgeving. Terminal Manager Wegens de recente promotie van een van de werknemers zijn zij voor een van de sites in de Haven van Antwerpen op zoek naar een Terminal Manager met gezonde ambitie die graag mee in de cockpit wil zitten van een dynamisch bedrijf in volle groei. * Als Terminal Manager speel je een sleutelrol in het bedrijf en zal jij via jouw kennis en inzet een belangrijke impact hebben op het bedrijf: Ideaal voor mensen die graag het verschil willen maken! * Plannen, coördineren en opvolgen van de dagelijkse operaties van de terminal die op een veilige, efficiënte en kosteneffectieve manier