Reistijd
... Min.
Sollicitatie methode
Taal van de job
Vaardigheden
Functiecategorie
Sector
Regio
Gemeente
Ervaringsniveau
Type contract
Voltijds/deeltijds
2 resultaten voor Chemisch laborant in Leuven binnen een straal van 30 km
){kind=logo}
Exxon Mobil Corporation * Machelen, Brussels,Belgium, BRU, BE * Contract duration unspecified * Full Time - Who are we? At ExxonMobil, our vision is to lead in energy innovations that advance modern living and a net-zero future. As one of the world's largest publicly traded energy and chemical companies, we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for. The success of our Upstream, Product Solutions and Low Carbon Solutions businesses is the result of the talent, curiosity and drive of our people. They bring solutions every day to optimize our strategy in energy, chemicals, lubricants and lower-emissions technologies. We invite you to bring your ideas to ExxonMobil to help create sustainable solutions that improve quality of life and meet society's evolving needs.
RentalTec Nv * Mechelen, Belgium * Contract duration unspecified * Full Time - Introduction - Job offers - Who we are - RentalTec provides its customers with short, medium and long term Rental and other OPEX (financial) solutions in order to fulfil and accelerate Testing, Measurement and Commissioning needs. RentalTec covers Telecom Installation & Maintenance (FTTH, 4G and 5G, Data Centres, IOT etc.), General purpose, RF & Microwave Development and Production Test, Power Quality Test, Energy Efficiency and all other possible types of Electronic Test and Measurement needs. With over 50 years' experience in the test and measurement Rental market, we provide the right tool for all personal testing needs and applications. Would you like to join our team? We are a rapidly growing company based in Mechelen – Belgium, Bensheim-Germany and Basingstoke-UK.
Deze jobs kunnen interessant zijn voor jou
){kind=logo}
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.
Jefferson Wells * RIXENSART * Contrat fixe à durée indéterminée * Plein temps - Brabant Wallon - Contracting - Vos responsabilités * Responsable d'organiser et exécuter des expériences de laboratoire upstream (culture cellulaire en adhérence in vitro) définies avec le en démontrant une expertise autant dans l'exécution que dans l'interprétation des résultats obtenus. * Faire preuve de séniorité en termes de résolution de problème, de polyvalence, d'organisation du travail et d'esprit critique. * Travailler principalement en laboratoire afin de pouvoir reproduire à petite échelle les étapes d'upstream de production de nos vaccins (culture cellulaire et tests in process associés), en participant aux tâches quotidiennes et en respectant les consignes de sécurité. * Ecriture des checklists de laboratoire électroniques et des rapports décrivant les objectifs et les résulta
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.
Representing the non-clinical safety team in cross-functional meetings * Good knowledge about non-clinical safety evaluation of starting materials, synthesis intermediates and impurities, degradation products, leachables and extractables and associated guidelines. Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Walloon – Brabant - Your responsibilities * Writing and monitoring risk assessments for impurities (eg, justification of specifications, elemental impurities risk assessments, extractables and leachables, degradation products, ICH M7-compliant evaluations, etc.) * Planning, coordinating and monitoring the conduct of toxicology studies at contract research organizations in line with project timelines and budget * Performing and monitoring toxicological risk assessments for various he
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
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
){kind=logo}
Research Scientist in Histology and Image Analysis for Neurodegenerative Diseases
Research Scientist in Histology and Image Analysis for Neurodegenerative Diseases
Jefferson Wells
Braine-l'Alleud
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
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
){kind=logo}
Snel solliciteren
Afin de rejoindre le département de Chimie de notre laboratoire de SGS Lab Simon à Wavre, nous sommes actuellement à la recherche d'un(e) « analyste en CHEMISTRY - PHYSICS » * Formation de niveau A1 (bachelier) en chimie analytique * Enregistre promptement, précisément et intégralement les données nécessaires à la traçabilité des opérations effectuées conformément aux procédures en vigueur (échantillons, réactifs, appareillages, initiales, dates) ; * Signale immédiatement tout résultat hors spécification au Team Leader conformément à la procédure en vigueur ; * Signale au plus vite au Team Leader tout besoin en matériel et réactifs ; * Respecte les procédures mises en vigueur, signale les écarts au Team Leader ; * Exp
){kind=logo}
Snel solliciteren
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.
Travailler principalement en laboratoire en réalisant des expériences analytiques, en participant aux tâches quotidiennes et en respectant les consignes de sécurité. * Ecriture des protocoles, checklists de laboratoire et des rapports décrivant la méthodologie et les résultats des expériences. * Bachelier/Master en Biochimie, Biologie moléculaire & cellulaire ou équivalent avec + de 3 ans d'expérience en laboratoire * Responsable de planifier, et des méthodes analytiques sur base de différentes familles de technologie (principalement tests d'infectivité sur cultures cellulaires en adhérence in vitro) en démontrant une expertise autant dans la planification, l'exécution que dans l'interprétation des résultats obtenus.
){kind=logo}
Als Laborant voer je metingen en conformiteitsanalysen uit met betrekking tot de kwaliteit van verschillende vloeibare petroleumproducten en chemicaliën (XRF, AAS, ICP-OES, ICP-MS, UV, motoren voor performantie, IR, GC,HPLC, chemische en fysische testen) met behulp van de meest modern uitgeruste laboratoriumapparatuur. Trefwoorden: labo, lab, laboratorium, chemie, analyse, inspectie, laborant, petrochemie - Stegmann Belgium (BVBA) * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Jouw verantwoordelijkheden - Daarnaast sta je ook in voor de controle en kalibratie van de toestellen die gebruikt worden, alsook de gehele netheid van het laboratorium. Specifieke verantwoordelijkheden • Je ontvangt de stalen in het laboratorium, meldt deze aan in het computerprogramma en genereert de werkorders. • Je voert specifieke analyses uit op
){kind=logo}
Snel solliciteren
SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - When you need to be sure, dat is waar SGS voor staat. Bij SGS bieden wij jou namelijk double layer sureness, dubbellaagse zekerheid. Als wereldleider op het gebied van inspectie, controle, analyse en certificering, staan wij garant voor kwaliteit en integriteit. Wereldwijd telt de SGS-familie bijna 100.000 enthousiaste medewerkers. In België geven ca 1900 collega's dagelijks het beste van zichzelf om onze klanten zo efficiënt en professioneel mogelijk verder te helpen. SGS heeft een indrukwekkende diversiteit aan diensten. Binnen onze divisie Industries & Environment hebben we o.a. een toonaangevend advies- en studiebureau dat gespecialiseerd is op het vlak van industrieel milieubeleid en veiligheidsstudies. We zoeken dus naar constructieve oplossingen en adviseren onze
As an Analytical Development – Document 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
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
Snel solliciteren
SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - SGS heeft een indrukwekkende diversiteit aan diensten, waaronder het IAC-labo (Institute for Applied Chromatography) dat gespecialiseerd is in hoogtechnologisch onderzoek. Het labo werd opgestart voor de bepaling van dioxines (stoffen die ongewenst kunnen ontstaan bij industriële processen zoals afvalverbranding en chemische productie en kunnen aangetroffen worden in de lucht, water en vervuilde bodem). Met ons onderzoek naar dergelijke persistente chemicaliën kunnen we identificeren waar dergelijke giftige concentraties ontstaan. Verder controleren we ook het dioxineniveau in voedsel en dierenvoeding. Maar onze portfolio werd ondertussen zeer sterk uitgebreid (PFAS, pesticiden, metalen, PCB's, detergenten, …). We identificeren ons binnen SGS als het 'specials' labo, wat
Snel solliciteren
Nous sommes actuellement à la recherche d'un(e) Analyste en Chimie pour rejoindre nos laboratoires SGS Lab Simon et SGS LCA. SGS Group Belgium * Wavre * Contrat fixe à durée indéterminée * Plein temps - Description de l'entreprise - SGS est une société internationale d'inspection, de vérification, de testing et de certification. Description du poste * Effectue les essais de conformité sur les matières premières ou produits finis. * Enregistre promptement, précisément et intégralement les données nécessaires à la traçabilité des opérations effectuées conformément aux procédures en vigueur (échantillons, réactifs, appareillages, initiales, dates). * Signale immédiatement tout résultat hors spécification au superviseur de laboratoire conformément à la procédure en vigueur. * Signale au plus vite au Team Leader tout besoin en matériel et réactifs. * Signa
Assurer la coordination de la validation des projets majeurs de TRD GMP en Drug Substance et Drug Product. * Assurer l'approche 'state of art' de la Validations du plan de validation (= stratégie de validation) jusqu'au Validation Summary Report, incluant : Ecriture, la revue et approbation de document de validation tels que les Risk Assessments, les protocoles IQ/OQ/PQ, les rapports IQ/OQ/PQ … * Expertise en validation IQ/OQ/PQ et GMP, solides connaissances en organisation matricielle et en gestion de projet. * Connaissance en validation de produit injectable. Jefferson Wells * RIXENSART * Contrat fixe à durée indéterminée * Plein temps - Consultance – Brabant Wallon - Vos responsabilités * Coordination de l'exécution des protocoles.
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
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
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
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
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