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    • genève, genève
    • temporary
    Avez-vous une première en qualification et/ou validation ? Connaissez-vous l’industrie stricte du médical ?Dans le cadre de l’augmentation des activités de notre client, un leader dans le domaine des dispositifs médicaux, nous recherchons un/e:Poste: Technicien(ne) qualification & validationLieu: GenèveDurée: Contrat temporaire jusqu'au 31.12.2022Vos tâches:Qualifier les équipements de production et les systèmes informatiques de production et du contrôle de qualité en conformité avec les guidelines et GMP internationales en vigueurRédiger des protocoles et des rapports de qualificationExécuter et renseigner les activités de qualification et de calibration (initiales / périodiques) des systèmesCoordonner et contrôler le déroulement des étapes de qualification dans les différents services concernésRevoir les résultats de qualification, renseigner les déviations associées et proposer des CAPAsMaintenir le niveau de qualification des systèmes et participer à l’amélioration continue de ceux-ci afin de garantir la Qualité des produits fabriquésÉvaluer tous signaux pouvant avoir un impact sur le niveau de qualification du site et en informer le responsable Qualification / ValidationVotre profil:Expérience en qualification de systèmes (équipements, utilités, informatique, stérilisation) dans un contexte GMPDiplôme en qualification-validation, automation, mécanique, électricité, maintenance ou génie climatiqueExpérience indispensable en industrie pharmaceutique et bonnes connaissances des GMP/BPF, connaissance des 21CFR210-211 et part 11 serait un plusFrançais et Anglais requisCette description vous intéresse ? Alors postulez vite sans attendre!
    Avez-vous une première en qualification et/ou validation ? Connaissez-vous l’industrie stricte du médical ?Dans le cadre de l’augmentation des activités de notre client, un leader dans le domaine des dispositifs médicaux, nous recherchons un/e:Poste: Technicien(ne) qualification & validationLieu: GenèveDurée: Contrat temporaire jusqu'au 31.12.2022Vos tâches:Qualifier les équipements de production et les systèmes informatiques de production et du contrôle de qualité en conformité avec les guidelines et GMP internationales en vigueurRédiger des protocoles et des rapports de qualificationExécuter et renseigner les activités de qualification et de calibration (initiales / périodiques) des systèmesCoordonner et contrôler le déroulement des étapes de qualification dans les différents services concernésRevoir les résultats de qualification, renseigner les déviations associées et proposer des CAPAsMaintenir le niveau de qualification des systèmes et participer à l’amélioration continue de ceux-ci afin de garantir la Qualité des produits fabriquésÉvaluer tous signaux pouvant avoir un impact sur le niveau de qualification du site et en informer le responsable Qualification / ValidationVotre profil:Expérience en qualification de systèmes (équipements, utilités, informatique, stérilisation) dans un contexte GMPDiplôme en qualification-validation, automation, mécanique, électricité, maintenance ou génie climatiqueExpérience indispensable en industrie pharmaceutique et bonnes connaissances des GMP/BPF, connaissance des 21CFR210-211 et part 11 serait un plusFrançais et Anglais requisCette description vous intéresse ? Alors postulez vite sans attendre!
    • wetteren, oost-vlaanderen
    • temporary
    • full-time
    Je helpt met het inpakken van de afgewerkte producten. Je voert kwaliteitscontrole uit van de afgewerkte producten.Je helpt bij het maken van de dozen om de afgewerkte producten in te pakken.
    Je helpt met het inpakken van de afgewerkte producten. Je voert kwaliteitscontrole uit van de afgewerkte producten.Je helpt bij het maken van de dozen om de afgewerkte producten in te pakken.
    • ghlin, hainaut
    • temporary
    • full-time
    En tant qu'opérateur de production, tes tâches principales seront les suivantes : - Emballage, pompage des matières premières et confection de solutions.- Contrôle et manutention des machines.- Analyse des matières premières, des échantillons et des produits finis.- Nettoyage des IBC's.- Respect des règles de sécurité et d'hygiène.- Travail administratif : formulaires à compléter, rapports à établir,...
    En tant qu'opérateur de production, tes tâches principales seront les suivantes : - Emballage, pompage des matières premières et confection de solutions.- Contrôle et manutention des machines.- Analyse des matières premières, des échantillons et des produits finis.- Nettoyage des IBC's.- Respect des règles de sécurité et d'hygiène.- Travail administratif : formulaires à compléter, rapports à établir,...
    • feluy, hainaut
    • temporary
    • full-time
    Tes responsabilités:- Calculer et analyser les mouvements des matières premières et des produits finis pour l'unité de production et préparer les indicateurs de performance en collaboration avec le responsable de production afin d'améliorer la rentabilité et la productivité.- Etablir divers rapports dans le cadre de la clôture mensuelle du budget et du plan décennal, afin notamment de mesurer les écarts avec le budget.- Participer à la création et à la maintenance de master data de SAP (références, codes articles, grades, recettes), afin que ce dernier soit en ligne avec l'activité de l'entreprise.- Assurer différentes tâches de support.- Respecter et appliquer les consignes en matière d'hygiène, de sécurité et d'environnement.
    Tes responsabilités:- Calculer et analyser les mouvements des matières premières et des produits finis pour l'unité de production et préparer les indicateurs de performance en collaboration avec le responsable de production afin d'améliorer la rentabilité et la productivité.- Etablir divers rapports dans le cadre de la clôture mensuelle du budget et du plan décennal, afin notamment de mesurer les écarts avec le budget.- Participer à la création et à la maintenance de master data de SAP (références, codes articles, grades, recettes), afin que ce dernier soit en ligne avec l'activité de l'entreprise.- Assurer différentes tâches de support.- Respecter et appliquer les consignes en matière d'hygiène, de sécurité et d'environnement.
    • thimister-clermont
    • temporary
    • full-time
    Tempo-team recherche des magasinier avec expérience en retract et frontal afin de travailler au magasin.Vous vous occupez du scanning de la marchandise, chargement, déchargement, rangement en rayons, ...
    Tempo-team recherche des magasinier avec expérience en retract et frontal afin de travailler au magasin.Vous vous occupez du scanning de la marchandise, chargement, déchargement, rangement en rayons, ...
    • ghislenghien, hainaut
    • temporary
    • full-time
    En tant que gestionnaire de paie, tu es chargé de:- paiement des salaires (congé, maladie, réducation ONNSS)- calculer les primes commerciales - indexer les salaires sur base du réglement de travail - répondre aux questions administratives- suivre les plannings- participer au projet RH
    En tant que gestionnaire de paie, tu es chargé de:- paiement des salaires (congé, maladie, réducation ONNSS)- calculer les primes commerciales - indexer les salaires sur base du réglement de travail - répondre aux questions administratives- suivre les plannings- participer au projet RH
    • upplands-bro kommun, stockholms län
    • temporary
    • heltid
    Randstad Life Sciences söker nu laboranter till vår kund i Brunna. Vi söker dig som är utbildad läkemedelstekniker eller har en kandidatexamen inom kemi eller motsvarande. Har du tidigare erfarenhet av att jobba i laborativ miljö enligt GMP är det meriterande. Du kommer att tillhöra sektionen för analys av råvaror där man ansvarar för kemiska analyser för att säkerställa kvaliteten på de inkomna och de egentillverkade råvarorna. Avdelningen utgör en viktig funktion för kvalitetskontrollen av råvaror som används i kundens tillverkning av läkemedel. Gruppen har cirka 14 medarbetare som arbetar nära varandra i team och har roligt på jobbet.Detta är ett konsultuppdrag med start omgående och sex månader framåt. För rätt person finns goda möjligheter för förlängning eller överrekrytering.Randstad Life Sciences är specialister inom naturvetenskap. Som konsult hos oss är det vi som är din arbetsgivare men du har din dagliga arbetsplats hos någon av våra kunder. Som konsult hos oss får du en trygg anställning med konkurrenskraftig fast lön, förmåner och kollektivavtalade villkor. Tillsammans med oss får du möjlighet att utvecklas och bredda din kompetens genom att vara ute på spännande uppdrag hos våra Life Science kunder. Hos Randstad Life Sciences står din personliga utveckling i fokus, och du erbjuds ett stort nätverk och många sociala aktiviteter.  Vi har vi även ett kompetenserbjudande som innebär att du har möjlighet att kompetensutveckla dig och/eller ta ut extra ledighet.
    Randstad Life Sciences söker nu laboranter till vår kund i Brunna. Vi söker dig som är utbildad läkemedelstekniker eller har en kandidatexamen inom kemi eller motsvarande. Har du tidigare erfarenhet av att jobba i laborativ miljö enligt GMP är det meriterande. Du kommer att tillhöra sektionen för analys av råvaror där man ansvarar för kemiska analyser för att säkerställa kvaliteten på de inkomna och de egentillverkade råvarorna. Avdelningen utgör en viktig funktion för kvalitetskontrollen av råvaror som används i kundens tillverkning av läkemedel. Gruppen har cirka 14 medarbetare som arbetar nära varandra i team och har roligt på jobbet.Detta är ett konsultuppdrag med start omgående och sex månader framåt. För rätt person finns goda möjligheter för förlängning eller överrekrytering.Randstad Life Sciences är specialister inom naturvetenskap. Som konsult hos oss är det vi som är din arbetsgivare men du har din dagliga arbetsplats hos någon av våra kunder. Som konsult hos oss får du en trygg anställning med konkurrenskraftig fast lön, förmåner och kollektivavtalade villkor. Tillsammans med oss får du möjlighet att utvecklas och bredda din kompetens genom att vara ute på spännande uppdrag hos våra Life Science kunder. Hos Randstad Life Sciences står din personliga utveckling i fokus, och du erbjuds ett stort nätverk och många sociala aktiviteter.  Vi har vi även ett kompetenserbjudande som innebär att du har möjlighet att kompetensutveckla dig och/eller ta ut extra ledighet.
    • ougrée, liege
    • temporary
    • 38 heures par semaine
    Starte ton job d'assistant de laboratoire étudiant chez notre partenaire à Liège. Dans ce cadre tu as pour mission de compléter les documents qui reprennent des informations concernant des essais agronomiques mis en place au cours des dernières saisons.
    Starte ton job d'assistant de laboratoire étudiant chez notre partenaire à Liège. Dans ce cadre tu as pour mission de compléter les documents qui reprennent des informations concernant des essais agronomiques mis en place au cours des dernières saisons.
    • solna kommun, stockholms län
    • temporary
    • fulltime
    Randstad Life Sciences are now looking for a Product Transfer Coordinator to join our team in Stockhholm. You will work with our client in Solna as part of their Process Life Cycle team (IVDR). The Process Life Cycle Team, a division of Product Transfer, acts as the technical partner to several Swedish and International functions within the organization. The team leads/coordinates post-launch changes, improvement projects, transfers of assays between manufacturing sites, and supports expansions into new markets. As part of these activities, they solve problems and develop new processes, methods and procedures, assuring manufacturability and continued production of cost-effective high-quality products. The position is temporary with start immediately and end on the 31st of January 2023.Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. 
    Randstad Life Sciences are now looking for a Product Transfer Coordinator to join our team in Stockhholm. You will work with our client in Solna as part of their Process Life Cycle team (IVDR). The Process Life Cycle Team, a division of Product Transfer, acts as the technical partner to several Swedish and International functions within the organization. The team leads/coordinates post-launch changes, improvement projects, transfers of assays between manufacturing sites, and supports expansions into new markets. As part of these activities, they solve problems and develop new processes, methods and procedures, assuring manufacturability and continued production of cost-effective high-quality products. The position is temporary with start immediately and end on the 31st of January 2023.Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. 
    • malmö kommun, skåne län
    • temporary
    • heltid
    Vill du vara med och förbättra kvalitén på läkemedel och medicintekniska produkter? Har du ett starkt driv och framåtanda och redo för att ta dig an kommande uppdrag hos våra Life Science-kunder i Skåne? Vi på Randstad Life Sciences vill till hösten utöka vårt konsultteam med ytterligare QA specialister. Vi söker dig med några eller många års erfarenhet av QA inom läkemedelsindustrin och/eller medicinteknisk industri. Som QA specialist hos oss får du möjligheten att hjälpa både våra större och mindre Life Science kunder i regionen och därmed bredda din erfarenhet inom QA området. Randstad Life Sciences är specialister inom naturvetenskap. Som konsult hos oss får du konkurrenskraftig lön, förmåner och kollektivavtalade villkor. Din konsultchef, som alltid finns nära till hands, ser till att du får varierande och utvecklande uppdrag på olika spännande företag i regionen. Hos Randstad Life Sciences står din personliga utveckling i fokus, och du erbjuds ett stort nätverk och många sociala aktiviteter.
    Vill du vara med och förbättra kvalitén på läkemedel och medicintekniska produkter? Har du ett starkt driv och framåtanda och redo för att ta dig an kommande uppdrag hos våra Life Science-kunder i Skåne? Vi på Randstad Life Sciences vill till hösten utöka vårt konsultteam med ytterligare QA specialister. Vi söker dig med några eller många års erfarenhet av QA inom läkemedelsindustrin och/eller medicinteknisk industri. Som QA specialist hos oss får du möjligheten att hjälpa både våra större och mindre Life Science kunder i regionen och därmed bredda din erfarenhet inom QA området. Randstad Life Sciences är specialister inom naturvetenskap. Som konsult hos oss får du konkurrenskraftig lön, förmåner och kollektivavtalade villkor. Din konsultchef, som alltid finns nära till hands, ser till att du får varierande och utvecklande uppdrag på olika spännande företag i regionen. Hos Randstad Life Sciences står din personliga utveckling i fokus, och du erbjuds ett stort nätverk och många sociala aktiviteter.
    • ninove, oost-vlaanderen
    • temporary
    • full-time
    Wat verwachten wij van jou als winkelverantwoordelijke? Een hele boterham, maar je krijgt er heel wat voor in de plaats!Op commercieel vlak heb je heel wat te bieden: -je staat in voor de klantentevredenheid en van de aantrekkelijkheid van de winkel-je staat in voor het onthaal van klanten in de winkel en aan de telefoon-je verleent advies over schoonheidsproducten en verkoopt deze ook op een aangename en professionele manier-je plant lokale commerciële acties en organiseert externe promo-actiesDaarnaast ben je ook verantwoordelijk voor de organisatie, demonstratie enuitvoering van je winkel:-je staat in voor een kwalitatief beheer van de stock-je staat in voor de bestellingen en de controle ervan-je staat in voor de inventaris, de planning en de taakverdeling van het winkelpersoneelBovenop dit alles ben je ook de ideale teammanager:-je kan een doelgericht en gemotiveerd team uitbouwen-je bent verantwoordelijk voor de communicatie binnen het team-je staat in voor het motiveren en evalueren van je teamleden-je volgt de opleidingsbehoeften van je medewerkers op en je staat in voor de opleidingsplannen
    Wat verwachten wij van jou als winkelverantwoordelijke? Een hele boterham, maar je krijgt er heel wat voor in de plaats!Op commercieel vlak heb je heel wat te bieden: -je staat in voor de klantentevredenheid en van de aantrekkelijkheid van de winkel-je staat in voor het onthaal van klanten in de winkel en aan de telefoon-je verleent advies over schoonheidsproducten en verkoopt deze ook op een aangename en professionele manier-je plant lokale commerciële acties en organiseert externe promo-actiesDaarnaast ben je ook verantwoordelijk voor de organisatie, demonstratie enuitvoering van je winkel:-je staat in voor een kwalitatief beheer van de stock-je staat in voor de bestellingen en de controle ervan-je staat in voor de inventaris, de planning en de taakverdeling van het winkelpersoneelBovenop dit alles ben je ook de ideale teammanager:-je kan een doelgericht en gemotiveerd team uitbouwen-je bent verantwoordelijk voor de communicatie binnen het team-je staat in voor het motiveren en evalueren van je teamleden-je volgt de opleidingsbehoeften van je medewerkers op en je staat in voor de opleidingsplannen
    • wetteren, oost-vlaanderen
    • temporary
    • full-time
    Jij bent het eerste aanspreekpunt om vragen te beantwoorden en problemen op te lossen van jouw collega gebruikers. Hierbij ga je klantgericht en oplossingsgericht te werk. Je probeert zo efficiënt mogelijk aan de slag te gaan. Je krijg hierbij enkel hulpmiddelen zoals interne documentie die je kan raadplegen en jouw collega's die mee gespecialiseerd zijn in bepaalde zaken. Hierbij werk je graag in team.
    Jij bent het eerste aanspreekpunt om vragen te beantwoorden en problemen op te lossen van jouw collega gebruikers. Hierbij ga je klantgericht en oplossingsgericht te werk. Je probeert zo efficiënt mogelijk aan de slag te gaan. Je krijg hierbij enkel hulpmiddelen zoals interne documentie die je kan raadplegen en jouw collega's die mee gespecialiseerd zijn in bepaalde zaken. Hierbij werk je graag in team.
    • stenungsund kommun, västra götaland
    • temporary
    • heltid
    LaboratorieteknikerVår världsledande kund i Stenungsund söker en driven laboratorietekniker till sitt driftlab. Driftlabbet utgör en servicefunktion som stöttar produktion med analyser på råvaror, mellanprodukter och renprodukter samt bidrar till att lösa driftproblem. Här erbjuds ett intressant och ansvarsfullt uppdrag i en växande modern industri. På driftlab jobbar i nuläget åtta personer med god sammanhållning och rak kommunikation. Gillar du en kombination av teknik, lagarbete och service är detta ett jobb för dig!
    LaboratorieteknikerVår världsledande kund i Stenungsund söker en driven laboratorietekniker till sitt driftlab. Driftlabbet utgör en servicefunktion som stöttar produktion med analyser på råvaror, mellanprodukter och renprodukter samt bidrar till att lösa driftproblem. Här erbjuds ett intressant och ansvarsfullt uppdrag i en växande modern industri. På driftlab jobbar i nuläget åtta personer med god sammanhållning och rak kommunikation. Gillar du en kombination av teknik, lagarbete och service är detta ett jobb för dig!
    • ghlin, hainaut
    • temporary
    • 38 heures par semaine
    Dans cette fonction, tu seras en charge de la logistique de différents contenants à l'aide d'un clarck frontal.L'essentiel de ton temps tu seras cariste en exterieur.
    Dans cette fonction, tu seras en charge de la logistique de différents contenants à l'aide d'un clarck frontal.L'essentiel de ton temps tu seras cariste en exterieur.
    • braine-l'alleud, brabant wallon
    • temporary
    • 38 heures par semaine
    Tu es titulaire d'un master en chimie ou en gestion de la production industrielle ? Tu possèdes des connaissances en gestion du personnel et en sécurité ? Tu recherches une fonction stimulante et remplie de défis avec un contrat CDI à la clé ? Randstad te propose une offre d'emploi comme chef d'équipe de production pour une entreprise située dans la région de Braine-l'alleud.Tes tâches principales en tant que Team Leader Production :- Tu organises le plan de production et tu veilles au respect des normes de sécurité et des procédures dans les ateliers- Tu gères le suivi et le déroulement des opérations de fabrication des produits en collaboration avec les chimistes et l¿équipe de production- Tu contribues au développement et à la formation continue de l'équipe afin que celle-ci devienne autonome- Tu communiques les informations importantes à l'équipe relatives au site et aux départements- Tu présentes le service par le biais d'audits en collaboration avec les chimistes et l'équipe de production aux autres entreprises- Tu sensibilises le personnel aux règles de sécurité, ainsi qu'à la pratique GMP et tu réalises une évaluation des risques dans les ateliers- Tu contribues à la vision de l'entreprise et à la culture d'amélioration en continue en utilisant les outils OPEX- Tu respectes le planning de production afin que les livraisons soient effectuées dans les délais
    Tu es titulaire d'un master en chimie ou en gestion de la production industrielle ? Tu possèdes des connaissances en gestion du personnel et en sécurité ? Tu recherches une fonction stimulante et remplie de défis avec un contrat CDI à la clé ? Randstad te propose une offre d'emploi comme chef d'équipe de production pour une entreprise située dans la région de Braine-l'alleud.Tes tâches principales en tant que Team Leader Production :- Tu organises le plan de production et tu veilles au respect des normes de sécurité et des procédures dans les ateliers- Tu gères le suivi et le déroulement des opérations de fabrication des produits en collaboration avec les chimistes et l¿équipe de production- Tu contribues au développement et à la formation continue de l'équipe afin que celle-ci devienne autonome- Tu communiques les informations importantes à l'équipe relatives au site et aux départements- Tu présentes le service par le biais d'audits en collaboration avec les chimistes et l'équipe de production aux autres entreprises- Tu sensibilises le personnel aux règles de sécurité, ainsi qu'à la pratique GMP et tu réalises une évaluation des risques dans les ateliers- Tu contribues à la vision de l'entreprise et à la culture d'amélioration en continue en utilisant les outils OPEX- Tu respectes le planning de production afin que les livraisons soient effectuées dans les délais
    • champlon
    • temporary
    • full-time
    Tu apprécies le travail en production.Tu effectues le triage du plastique et l'approvisionnement de la ligne de production.
    Tu apprécies le travail en production.Tu effectues le triage du plastique et l'approvisionnement de la ligne de production.
    • fortaleza, ceara
    • temporary
    • R$500 - R$1,500 per month
    Controlar as informações de compra e entrega de materiais e medicamentos. Checar estoque físico e virtual. Gerar relatórios de perdas. Auxiliar farmacêuticos no controle dos níveis de estoque. Realizar contagem de estoque. Administrar validade dos materiais e medicamentos. Remanejar itens entre estoques.
    Controlar as informações de compra e entrega de materiais e medicamentos. Checar estoque físico e virtual. Gerar relatórios de perdas. Auxiliar farmacêuticos no controle dos níveis de estoque. Realizar contagem de estoque. Administrar validade dos materiais e medicamentos. Remanejar itens entre estoques.
    • fortaleza, ceara
    • temporary
    • R$500 - R$1,500 per month
    RESPONSAVEL BAIXA DE VALES, CARTA DE TROCA,SOLICITAÇÃO E DISPENSAÇÃO DE EMPRESTIMO PARA OPUTRAS EMPRESAS, MAPA DE CANVAS PACIENTE TRAQUEOSTOMO, BATER ESTOQUE PEDIDO SEMANAL ONCOLOGIA, CONTAGENS, CONFERENCIAS, INVENTARIOS DE LOTE CONTROLE DE ESTOQUE.
    RESPONSAVEL BAIXA DE VALES, CARTA DE TROCA,SOLICITAÇÃO E DISPENSAÇÃO DE EMPRESTIMO PARA OPUTRAS EMPRESAS, MAPA DE CANVAS PACIENTE TRAQUEOSTOMO, BATER ESTOQUE PEDIDO SEMANAL ONCOLOGIA, CONTAGENS, CONFERENCIAS, INVENTARIOS DE LOTE CONTROLE DE ESTOQUE.
    • tullamore, offaly
    • temporary
    • €30,000 - €35,000 per year
    • full-time
    Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Company Profile:65+ years of experience in healthNearly $6 billion annual revenues25 manufacturing sites around the world10,000 employees worldwide of which 1,100 employees are committed to R&DGiven the large expansion currently underway, there are great opportunities for progression within this global company. Process Scientist summary & requirements : The role of this key team member within the Production Department will assist with the development and validation of processes for recombinant antibodies for veterinary use. This will include working with teams both on site and externally with Contract Manufacturing Organisations for some of the process development activity and technical transfer of the process into and out of the facility in Offaly. This is a cross functional role in that it will cover work in both upstream and downstream activities. Key Responsibilities:To support the development, optimisation, scale-up and validation of all upstream steps in a monoclonal antibody production process. Work with external partners to provide the necessary technical support for successful completion of projects including the transfer of processes into the facility.Strict adherence to GMP, working in a cleanroom environment and executing batch records.Support the writing and updating of Batch Manufacturing Records, SOPs, and other quality documents required for GMP manufacture.Provide hands-on support for all manufacturing activities including buffer / media preparation, cell culture and bioreactor process steps. Provide technical input and support writing of technical reports required for regulatory purposesParticipate in Quality and Safety regulatory audits and completion of deviations and investigations into non-conformance's.Identify continuous improvement initiatives and action plans to implement operational excellence and lean practices. Manufacture products using cell culture techniques Qualification and Experience: M.Sc. or B.Sc in Chemical/Biochemical Engineering or related Biological Sciences with ≥ 1 years of industrial experience preferably. Basic mammalian cell culture experience including thawing, culturing, cell counting.Experience using SAP and Trackwise/ETS would be highly advantageous. Hands-on experience of bioreactors such as WAVE and Xcellerex or equivalent systems desirable.Experience in scale up of bioprocesses from bench scale to large scale.Working in a controlled regulated environment e.g. GMP/GLPKnowledge of analytical methods required for cell culture/protein characterisation. Experience with deviation investigations and CAPA implementation would be highly advantageous. Knowledge of key suppliers of process materials and equipment including disposable systems.Excellent verbal and written communication skills. Ability to maintain very clear records of work completed. Production Operators summary and requirements : The role of this key team member within the Manufacturing Department will include responsibility for the manufacture and validation of processes for recombinant antibodies for veterinary use. This will include working with teams, both on the Offaly site and externally with Contract Manufacturing Organisations for some of the process development activity, and for technical transfer of the process into the client's facility. Reporting Structure Reporting to the Manufacturing Manager Duties & Responsibilities Job-Specific Duties may include but are not limited to: Documentation: P.O. generation and ordering for manufacturing to support production batches * Assist with writing SOPs and Forms. Record data and log activities according to cGMP standards. Production Activities: Calibration, set-up and use of production equipment including - autoclave, balances, pH and conductivity meters, osmometers, Blood Gas Analysers and peristaltic pumps.Prepare solutions, including buffers, reagents, and cell culture media and related tasks including but not limited to pH titration, osmolality adjustment, sterile filtration techniques, and sampling. Prepare and operate equipment according to written procedures (SOPs) Assist with setting up the GMP areas for batch production including received materials, stock counts and performing cleaning tasks. Sanitization of the WFI loopPerform routine WFI sampling for Production. Log production samples to QC. May include cross training in additional functional areas such as inventory management services. Accountability: Perform all duties with a high level of honesty and integrity and adhere to all site safety, environmental and quality policies on site. Based on business needs, weekend work may be required. POSITION SPECIFICATION Qualifications, Experience, Skills, Knowledge and Attributes Leaving Cert or Equivalent. Applicants with Higher Certificates (NFQ Level 6) or Ordinary Bachelor's degrees (NFQ Level 7) in science-related fields would be advantageous. GMP experience would be a distinct advantage. Basic use of MS office. * All applicants must have competence in spoken and written English.Randstad Financial & Professional encourage applications from individuals of all ages & backgrounds. Appointment will be made on merit alone but candidates must be able to demonstrate their ability to work in the UK. Randstad Financial & Professional acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
    Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Company Profile:65+ years of experience in healthNearly $6 billion annual revenues25 manufacturing sites around the world10,000 employees worldwide of which 1,100 employees are committed to R&DGiven the large expansion currently underway, there are great opportunities for progression within this global company. Process Scientist summary & requirements : The role of this key team member within the Production Department will assist with the development and validation of processes for recombinant antibodies for veterinary use. This will include working with teams both on site and externally with Contract Manufacturing Organisations for some of the process development activity and technical transfer of the process into and out of the facility in Offaly. This is a cross functional role in that it will cover work in both upstream and downstream activities. Key Responsibilities:To support the development, optimisation, scale-up and validation of all upstream steps in a monoclonal antibody production process. Work with external partners to provide the necessary technical support for successful completion of projects including the transfer of processes into the facility.Strict adherence to GMP, working in a cleanroom environment and executing batch records.Support the writing and updating of Batch Manufacturing Records, SOPs, and other quality documents required for GMP manufacture.Provide hands-on support for all manufacturing activities including buffer / media preparation, cell culture and bioreactor process steps. Provide technical input and support writing of technical reports required for regulatory purposesParticipate in Quality and Safety regulatory audits and completion of deviations and investigations into non-conformance's.Identify continuous improvement initiatives and action plans to implement operational excellence and lean practices. Manufacture products using cell culture techniques Qualification and Experience: M.Sc. or B.Sc in Chemical/Biochemical Engineering or related Biological Sciences with ≥ 1 years of industrial experience preferably. Basic mammalian cell culture experience including thawing, culturing, cell counting.Experience using SAP and Trackwise/ETS would be highly advantageous. Hands-on experience of bioreactors such as WAVE and Xcellerex or equivalent systems desirable.Experience in scale up of bioprocesses from bench scale to large scale.Working in a controlled regulated environment e.g. GMP/GLPKnowledge of analytical methods required for cell culture/protein characterisation. Experience with deviation investigations and CAPA implementation would be highly advantageous. Knowledge of key suppliers of process materials and equipment including disposable systems.Excellent verbal and written communication skills. Ability to maintain very clear records of work completed. Production Operators summary and requirements : The role of this key team member within the Manufacturing Department will include responsibility for the manufacture and validation of processes for recombinant antibodies for veterinary use. This will include working with teams, both on the Offaly site and externally with Contract Manufacturing Organisations for some of the process development activity, and for technical transfer of the process into the client's facility. Reporting Structure Reporting to the Manufacturing Manager Duties & Responsibilities Job-Specific Duties may include but are not limited to: Documentation: P.O. generation and ordering for manufacturing to support production batches * Assist with writing SOPs and Forms. Record data and log activities according to cGMP standards. Production Activities: Calibration, set-up and use of production equipment including - autoclave, balances, pH and conductivity meters, osmometers, Blood Gas Analysers and peristaltic pumps.Prepare solutions, including buffers, reagents, and cell culture media and related tasks including but not limited to pH titration, osmolality adjustment, sterile filtration techniques, and sampling. Prepare and operate equipment according to written procedures (SOPs) Assist with setting up the GMP areas for batch production including received materials, stock counts and performing cleaning tasks. Sanitization of the WFI loopPerform routine WFI sampling for Production. Log production samples to QC. May include cross training in additional functional areas such as inventory management services. Accountability: Perform all duties with a high level of honesty and integrity and adhere to all site safety, environmental and quality policies on site. Based on business needs, weekend work may be required. POSITION SPECIFICATION Qualifications, Experience, Skills, Knowledge and Attributes Leaving Cert or Equivalent. Applicants with Higher Certificates (NFQ Level 6) or Ordinary Bachelor's degrees (NFQ Level 7) in science-related fields would be advantageous. GMP experience would be a distinct advantage. Basic use of MS office. * All applicants must have competence in spoken and written English.Randstad Financial & Professional encourage applications from individuals of all ages & backgrounds. Appointment will be made on merit alone but candidates must be able to demonstrate their ability to work in the UK. Randstad Financial & Professional acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
    • willebroek, antwerpen
    • temporary
    • €15.50 per hour
    • 38 uren per week
    Je gaat als magazijnier aan de slag bij Imerys op hun site in Willebroek, in daguren en aan een verloning van 15,50 euro/uur. Je komt terecht in het magazijn dat verbonden is aan de productie site waar ze carbon black maken, een additief voor polymeren of lithiumbatterijen. Jij zal instaan voor het magazijnbeheer, klaarzetten van bestellingen en het stockbeheer.
    Je gaat als magazijnier aan de slag bij Imerys op hun site in Willebroek, in daguren en aan een verloning van 15,50 euro/uur. Je komt terecht in het magazijn dat verbonden is aan de productie site waar ze carbon black maken, een additief voor polymeren of lithiumbatterijen. Jij zal instaan voor het magazijnbeheer, klaarzetten van bestellingen en het stockbeheer.
    • södertälje kommun, stockholms län
    • temporary
    • fulltime
    Third Party Supplier (3PS) CMC Associate, Global Regulatory ExcellenceAre you an organized and detail-oriented person who enjoys working with documentation? Do you have experience from working with quality in the pharmaceutical industry?  This might be the next challenge for you!AstraZeneca is operating as a supplier for divested products where the manufacturing licence is now owned by an external partner.  As part of this relationship there is a requirement to ensure that AstraZeneca manufacturing network has full visibility and access to the current regulatory approved Chemistry Manufacturing and Controls (CMC) dossier for each country where the product is marketed. This is critical in ensuring that products are manufactured in compliance with the licences held by the third party licence holder. We are looking for 3PS CMC Associate to join our CMC team focused on divestment related activities located in Södertälje. As a consultant at Randstad Life Sciences, we are your employer, but you have your daily workplace with one of our customers. Your consulting manager is always close at hand, both during and between assignments to help you develop your career in the direction you dream of. As a consultant with us, you get a competitive salary, benefits and collectively agreed terms. We are responsive to your wishes regarding assignments and tasks and with our broad customer portfolio in Mälardalen, we will together adapt your continued career according to your skills, experience and ambition. At Randstad Life Sciences, we have an offer that means that you have the opportunity to develop your skills and / or take extra time off after you have been with us for a while. You will be part of a larger consulting team within Life Sciences and have the opportunity to broaden your network and gain valuable experience from different workplaces.
    Third Party Supplier (3PS) CMC Associate, Global Regulatory ExcellenceAre you an organized and detail-oriented person who enjoys working with documentation? Do you have experience from working with quality in the pharmaceutical industry?  This might be the next challenge for you!AstraZeneca is operating as a supplier for divested products where the manufacturing licence is now owned by an external partner.  As part of this relationship there is a requirement to ensure that AstraZeneca manufacturing network has full visibility and access to the current regulatory approved Chemistry Manufacturing and Controls (CMC) dossier for each country where the product is marketed. This is critical in ensuring that products are manufactured in compliance with the licences held by the third party licence holder. We are looking for 3PS CMC Associate to join our CMC team focused on divestment related activities located in Södertälje. As a consultant at Randstad Life Sciences, we are your employer, but you have your daily workplace with one of our customers. Your consulting manager is always close at hand, both during and between assignments to help you develop your career in the direction you dream of. As a consultant with us, you get a competitive salary, benefits and collectively agreed terms. We are responsive to your wishes regarding assignments and tasks and with our broad customer portfolio in Mälardalen, we will together adapt your continued career according to your skills, experience and ambition. At Randstad Life Sciences, we have an offer that means that you have the opportunity to develop your skills and / or take extra time off after you have been with us for a while. You will be part of a larger consulting team within Life Sciences and have the opportunity to broaden your network and gain valuable experience from different workplaces.
    • södertälje kommun, stockholms län
    • temporary
    • fulltime
    CMC Regulatory Affairs Associate, Global Regulatory ExcellenceAre you an organized and detail-oriented person who enjoys working with documentation? Do you have experience from working with quality in the pharmaceutical industry?  This might be the next challenge for you! CMC Regulatory Affairs is a global function that manages all Chemistry, Manufacturing and Controls (CMC) regulatory activities across AstraZeneca’s global supply chain. We are looking for CMC Regulatory Affairs Associates to join our CMC team focused on divestment related activities located in Södertälje. We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join us and be part of an extraordinary place to work; an environment that energizes and empowers each of us to support compliant product supply through partnership with other AZ teams.As a consultant at Randstad Life Sciences, we are your employer, but you have your daily workplace with one of our customers. Your consulting manager is always close at hand, both during and between assignments to help you develop your career in the direction you dream of. As a consultant with us, you get a competitive salary, benefits and collectively agreed terms. We are responsive to your wishes regarding assignments and tasks and with our broad customer portfolio in Mälardalen, we will together adapt your continued career according to your skills, experience and ambition. At Randstad Life Sciences, we have an offer that means that you have the opportunity to develop your skills and / or take extra time off after you have been with us for a while. You will be part of a larger consulting team within Life Sciences and have the opportunity to broaden your network and gain valuable experience from different workplaces.
    CMC Regulatory Affairs Associate, Global Regulatory ExcellenceAre you an organized and detail-oriented person who enjoys working with documentation? Do you have experience from working with quality in the pharmaceutical industry?  This might be the next challenge for you! CMC Regulatory Affairs is a global function that manages all Chemistry, Manufacturing and Controls (CMC) regulatory activities across AstraZeneca’s global supply chain. We are looking for CMC Regulatory Affairs Associates to join our CMC team focused on divestment related activities located in Södertälje. We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join us and be part of an extraordinary place to work; an environment that energizes and empowers each of us to support compliant product supply through partnership with other AZ teams.As a consultant at Randstad Life Sciences, we are your employer, but you have your daily workplace with one of our customers. Your consulting manager is always close at hand, both during and between assignments to help you develop your career in the direction you dream of. As a consultant with us, you get a competitive salary, benefits and collectively agreed terms. We are responsive to your wishes regarding assignments and tasks and with our broad customer portfolio in Mälardalen, we will together adapt your continued career according to your skills, experience and ambition. At Randstad Life Sciences, we have an offer that means that you have the opportunity to develop your skills and / or take extra time off after you have been with us for a while. You will be part of a larger consulting team within Life Sciences and have the opportunity to broaden your network and gain valuable experience from different workplaces.
    • engis, liege
    • temporary
    • 38 heures par semaine
    Starte ton job comme assistant qualité chez notre partenaire, à la renommée internationale dans le monde de la chimie ! Un bachelier scientifique ? Des connaissances en chimie ? Tu es une personne dynamique et ouverte ? Alors tu es certainement le nouveau membre de l'équipe qualité de Liège ! En tant que tel, tu es assistant qualité, sécurité et environnement et tes responsabilités sont les suivantes sur le site de Liège :- Gestion des questionnaires clients et des demandes d'extension durée de vie des produits,- Création des attestations clients et standards,- Assurer l'étiquetage client,- Respect et faire respecter les consignes de sécurité, d'environnement et de qualité.
    Starte ton job comme assistant qualité chez notre partenaire, à la renommée internationale dans le monde de la chimie ! Un bachelier scientifique ? Des connaissances en chimie ? Tu es une personne dynamique et ouverte ? Alors tu es certainement le nouveau membre de l'équipe qualité de Liège ! En tant que tel, tu es assistant qualité, sécurité et environnement et tes responsabilités sont les suivantes sur le site de Liège :- Gestion des questionnaires clients et des demandes d'extension durée de vie des produits,- Création des attestations clients et standards,- Assurer l'étiquetage client,- Respect et faire respecter les consignes de sécurité, d'environnement et de qualité.
    • mölndal kommun, västra götaland
    • temporary
    • fulltime
    Senior Research Scientist – In vitro cardiac disease modellingAre you an experienced scientist in the field of stem cells and gene editing? Would you like to contribute to the development of novel therapies? This might be the next challenge for you!At AstraZeneca in Gothenburg, Sweden we have an exciting opportunity for you to join us in Applied Stem Cell Sciences group in Translational Genomics, Discovery Sciences, Biopharmaceuticals R&D, as a bench-based Senior Research Scientist to be a key player in developing therapeutics to change patients’ lives.
    Senior Research Scientist – In vitro cardiac disease modellingAre you an experienced scientist in the field of stem cells and gene editing? Would you like to contribute to the development of novel therapies? This might be the next challenge for you!At AstraZeneca in Gothenburg, Sweden we have an exciting opportunity for you to join us in Applied Stem Cell Sciences group in Translational Genomics, Discovery Sciences, Biopharmaceuticals R&D, as a bench-based Senior Research Scientist to be a key player in developing therapeutics to change patients’ lives.
    • tullamore, offaly
    • temporary
    • part-time
    Position Title Site Quality Systems LeadDepartment Quality Assurance Role PurposeThe Site Quality Systems Lead will manage and oversee the quality management system to assure the site is ICH Q10 compliant. Quality Systems lead will ensure lean efficient quality systems and tools are implemented to monitor and maintain the site QMS including GMP readiness and site audit preparation. In addition, ensure the site is complaint to EU and FDA regulations and that Systems, Standard Operating Procedures and tools are in place to ensure compliance to cGMP through ongoing training, process review and monitoring of Key Performance and Quality Indicators.Reporting StructureReporting to The Senior Quality Operations Manager. Duties & ResponsibilitiesAssume a lead role in the oversight and maintenance of the Quality Management Systems identifying areas for improvement & optimisation to support operational and release functions.Monitor and report Quality Systems & Standards implementation progress, notifying any predicted shortfall or discrepancies against timescale and budgets.Review and approve of site documentation including SOPs, Reports, Protocols to ensure compliance.Review and approval of non-conformance reports including deviations, laboratory investigations & environmental excursions to ensure compliance and timely closure.Responsible for site quality system governance through management review to ensure its continuing suitability and effectiveness.Responsible for running & coordination of site quality council meetings and presentation of trends, data and performance versus site and platform quality metrics.Through Key Quality Performance Indicator Dashboard, monitor site quality systems performance to ensure they consistently remain in place, in use and in control, comply with Global Quality Policies and Standards and meet the most current regulatory requirements and best industry practices.Participate in Site regulatory inspections, internal audit program and vendor audits. Set up and implement associated remediation and continuous improvement programs on time in full and monitor CAPA effectiveness.Participate in or lead internal and external audits including 3rd party audits and supplier reviews.Interface with other departments such as Engineering, Laboratories, Operations, Warehouse and Process Development to ensure quality objectives are understood and achieved.Ownership and oversight of site Change Control Process to ensure implementation of change control activities in accordance with site procedures.Implementation of the site risk management process and maintenance of Site Risk Register.Develop and where appropriate deliver training across the teams regarding the quality topics and metrics.SME and key point of contact on quality systems such as deviations, CAPA's and change controls.Oversee site training programmeMaintains a contemporary understanding of cGMP regulations and guidance in relation to all aspects of validation across manufacturing, laboratories and facilities.Partake in or lead periodic quality review meetings to ensure compliance and continuous improvement.Support the development of quality goals and targets as part of the organisation's strategic plan.Write or assist in writing, reviewing and approval of SOPs and other GMP documents.Ensure GMP documentation is properly managed and archived.Serve as a quality culture role model and instil a strong quality and compliance culture across the site. Randstad Financial & Professional encourage applications from individuals of all ages & backgrounds. Appointment will be made on merit alone but candidates must be able to demonstrate their ability to work in the UK. Randstad Financial & Professional acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
    Position Title Site Quality Systems LeadDepartment Quality Assurance Role PurposeThe Site Quality Systems Lead will manage and oversee the quality management system to assure the site is ICH Q10 compliant. Quality Systems lead will ensure lean efficient quality systems and tools are implemented to monitor and maintain the site QMS including GMP readiness and site audit preparation. In addition, ensure the site is complaint to EU and FDA regulations and that Systems, Standard Operating Procedures and tools are in place to ensure compliance to cGMP through ongoing training, process review and monitoring of Key Performance and Quality Indicators.Reporting StructureReporting to The Senior Quality Operations Manager. Duties & ResponsibilitiesAssume a lead role in the oversight and maintenance of the Quality Management Systems identifying areas for improvement & optimisation to support operational and release functions.Monitor and report Quality Systems & Standards implementation progress, notifying any predicted shortfall or discrepancies against timescale and budgets.Review and approve of site documentation including SOPs, Reports, Protocols to ensure compliance.Review and approval of non-conformance reports including deviations, laboratory investigations & environmental excursions to ensure compliance and timely closure.Responsible for site quality system governance through management review to ensure its continuing suitability and effectiveness.Responsible for running & coordination of site quality council meetings and presentation of trends, data and performance versus site and platform quality metrics.Through Key Quality Performance Indicator Dashboard, monitor site quality systems performance to ensure they consistently remain in place, in use and in control, comply with Global Quality Policies and Standards and meet the most current regulatory requirements and best industry practices.Participate in Site regulatory inspections, internal audit program and vendor audits. Set up and implement associated remediation and continuous improvement programs on time in full and monitor CAPA effectiveness.Participate in or lead internal and external audits including 3rd party audits and supplier reviews.Interface with other departments such as Engineering, Laboratories, Operations, Warehouse and Process Development to ensure quality objectives are understood and achieved.Ownership and oversight of site Change Control Process to ensure implementation of change control activities in accordance with site procedures.Implementation of the site risk management process and maintenance of Site Risk Register.Develop and where appropriate deliver training across the teams regarding the quality topics and metrics.SME and key point of contact on quality systems such as deviations, CAPA's and change controls.Oversee site training programmeMaintains a contemporary understanding of cGMP regulations and guidance in relation to all aspects of validation across manufacturing, laboratories and facilities.Partake in or lead periodic quality review meetings to ensure compliance and continuous improvement.Support the development of quality goals and targets as part of the organisation's strategic plan.Write or assist in writing, reviewing and approval of SOPs and other GMP documents.Ensure GMP documentation is properly managed and archived.Serve as a quality culture role model and instil a strong quality and compliance culture across the site. Randstad Financial & Professional encourage applications from individuals of all ages & backgrounds. Appointment will be made on merit alone but candidates must be able to demonstrate their ability to work in the UK. Randstad Financial & Professional acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
    • bornem, antwerpen
    • temporary
    • €15.00 per hour
    • 38 uren per week
    Zin in een tijdelijke administratieve uitdaging voor een viertal maanden? Voor Lonza zijn we op zoek naar een administratieve planning assistent die meewerkt met diverse administratieve taken. Hieronder valt o.a. werken met SAP, werken met verschillende reporting tools en het zelfstandig administratief opvolgen van klanten.
    Zin in een tijdelijke administratieve uitdaging voor een viertal maanden? Voor Lonza zijn we op zoek naar een administratieve planning assistent die meewerkt met diverse administratieve taken. Hieronder valt o.a. werken met SAP, werken met verschillende reporting tools en het zelfstandig administratief opvolgen van klanten.
    • bornem, antwerpen
    • temporary
    • €15.00 per hour
    • 40 uren per week
    Interesse in een tijdelijke uitdaging bij een internationale speler? Kans op verlenging en vast contract mogelijk.Als customer service medewerker bestaat het takenpakket uit:- Orders ingeven in een ERP (SAP) systeem en dit bevestigen naar de klant- Opvolgen van orders- Klanten informeren over het aanbod van producten: prijzen, beschikbaarheid, ...- Klachtbehandeling- Analyses en rapportering uitvoeren
    Interesse in een tijdelijke uitdaging bij een internationale speler? Kans op verlenging en vast contract mogelijk.Als customer service medewerker bestaat het takenpakket uit:- Orders ingeven in een ERP (SAP) systeem en dit bevestigen naar de klant- Opvolgen van orders- Klanten informeren over het aanbod van producten: prijzen, beschikbaarheid, ...- Klachtbehandeling- Analyses en rapportering uitvoeren
    • renaix
    • temporary
    • full-time
    En tant qu'opérateur machine, tu es responsable d'une machine de production complexe:- tu suis le planning de production et paramètres la machine sur bases des spécifications des clients- tu alimentes la machine en matières premières - tu contrôles la production avec rigueur et précision: températures, quantités, etc- tu interviens en cas de blocage ou de panne de 1e niveau (compétences mécaniques/électriques)- tu gères les problèmes de qualité sur la production en adaptant les paramètres
    En tant qu'opérateur machine, tu es responsable d'une machine de production complexe:- tu suis le planning de production et paramètres la machine sur bases des spécifications des clients- tu alimentes la machine en matières premières - tu contrôles la production avec rigueur et précision: températures, quantités, etc- tu interviens en cas de blocage ou de panne de 1e niveau (compétences mécaniques/électriques)- tu gères les problèmes de qualité sur la production en adaptant les paramètres
    • diegem, vlaams-brabant
    • temporary
    • 38 uren per week
    Als Digital Marketeer geniet je van een gevarieerd takenpakket met verschillende verantwoordelijkheden. Wat betekent dat concreet?- website management voor de verschillende merken van het bedrijf- onderhouden van de sociale mediapagina's- e-mail marketingcampagnes naar interne en externe stakeholders- coordineren van de digitale salesactiviteiten- beheren van het B2B dataverkeer via het online bestelplatform- analyseren en rapporteren van data en resultaten- af en toe zal je ook mee ingezet worden voor de organisatie van events
    Als Digital Marketeer geniet je van een gevarieerd takenpakket met verschillende verantwoordelijkheden. Wat betekent dat concreet?- website management voor de verschillende merken van het bedrijf- onderhouden van de sociale mediapagina's- e-mail marketingcampagnes naar interne en externe stakeholders- coordineren van de digitale salesactiviteiten- beheren van het B2B dataverkeer via het online bestelplatform- analyseren en rapporteren van data en resultaten- af en toe zal je ook mee ingezet worden voor de organisatie van events
    • grobbendonk, antwerpen
    • temporary
    • 38 uren per week
    Voor onze klant in Grobbendonk, een toonaangevend kunststofproductiebedrijf, zijn wij op zoek naar een voltijds administratief bediende ter ondersteuning van de boekhouding. Het gaat om een tijdelijke opdracht van 1 jaar met kans op verlenging. Een 4/5de tewerkstelling is ook bespreekbaar.Jouw takenpakket:- Je staat in voor nakijken van facturen- Je voert data in in het computersysteem- Je scant documenten in- Je klasseert documenten- Je geeft orders in in het computersysteem- Je bent verantwoordelijk voor de inkomende telefonie en schakelt klanten door naar de juiste contactpersoon
    Voor onze klant in Grobbendonk, een toonaangevend kunststofproductiebedrijf, zijn wij op zoek naar een voltijds administratief bediende ter ondersteuning van de boekhouding. Het gaat om een tijdelijke opdracht van 1 jaar met kans op verlenging. Een 4/5de tewerkstelling is ook bespreekbaar.Jouw takenpakket:- Je staat in voor nakijken van facturen- Je voert data in in het computersysteem- Je scant documenten in- Je klasseert documenten- Je geeft orders in in het computersysteem- Je bent verantwoordelijk voor de inkomende telefonie en schakelt klanten door naar de juiste contactpersoon
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