Die PHARCONA GmbH ist ein mittelständisches Unternehmen im westlichen Münsterland, das kosmetische Produkte sowie Nahrungsergänzungsmittel entwickelt, herstellt und vertreibt. Zur Verstärkung unsers Teams suchen wir zum nächstmöglichen Zeitpunkt eine/n Maschinenführer (m/w/d) Ihre Aufgabenschwerpunkte: - Bedienen, Einrichten und Steuern von Produktions- und Verpackungslinien - Abfüllung und Konfektionierung von Produkten - Fehleranalyse und Behebung von Produktionsstörungen - Qualitätssichernde Maßnahmen - Reinigung und Desinfektion der Maschinen und des Produktionsumfelds - Einhaltung/Umsetzung jeglicher Arbeitssicherheits- und Hygienevorschriften - Durchführung und Dokumentation der Inprozesskontrollen - Mitarbeiterführung und Einarbeitung neuer Mitarbeiter Unser Anforderungsprofil: - Sie haben eine abgeschlossene Ausbildung im technischen Bereich oder haben Berufserfahrung als Maschinenführer im Lebensmittelbereich - Sie arbeiten teamorientiert, eigenverantwortlich und denken qualitätsbewusst - Sie besitzen ein hohes Maß an Flexibilität und die Bereitschaft zur Schichtarbeit (Früh,- Spät,- Nachtschicht) Wir bieten: • einen anspruchsvollen und abwechslungsreichen Aufgabenbereich in Zusammenarbeit mit der Produktions- und Betriebsleitung • ein gutes Arbeitsklima in einem motivierten Team • schnelle Entscheidungswege • einen sicheren Arbeitsplatz in einem modernen Unternehmen Haben wir Ihr Interesse geweckt? Dann erwarten Sie ein leistungsstarkes, motiviertes Team sowie ein modernes und innovatives Unternehmen mit abwechslungsreichen Aufgaben und Entwicklungsmöglichkeiten. Unser Team freut sich auf Ihre Bewerbung! Bitte richten Sie Ihre Bewerbungsunterlagen an: PHARCONA GmbH, Benzstraße 1, 48683 Ahaus, www.pharcona.de Oder gerne auch per Mail an: bewerbung@pharcona.de Ergänzende Informationen: Anforderungen an den Bewerber: Erweiterte Kenntnisse: Maschinenführung, Anlagenführung, -bedienung, Qualitätsprüfung, Qualitätssicherung

Машинните оператори в химическото производство наблюдават и обслужват машини и съоръжения за смесване, разбъркване, преработване и опаковане на разнообразни химически продукти.

1 Drug Product Project Leader (m/f/d) - Associate Director Science & Technology Job ID REQ-10065090LOCATION: Schaftenau, Austria ROLE TYPE: Hybrid Working, #LI-Hybrid Join our global team of highly skilled Drug Product Project Leaders with presence in all technical research and development sites for Biologics at Novartis! We seek an experienced, curious and resilient leader to drive the late-stage drug product development of our biologics product pipeline. As Drug Product Project Leader in Austria, you will be the strategic lead of drug product development of Biologics and be accountable for agreed upon deliverables to the CMC team. Enjoy an inspired environment with a clear purpose in an impactful role - bringing innovation to patients and to the market!About the RoleYour responsibilities include:  * Lead the technical development strategy for complex biologics, representing Drug Product Development in the global Chemistry Manufacturing Controls (CMC) team and ensuring delivery of agreed milestones  * Champion scientific excellence in the CMC team regarding drug product formulation and process development, technical transfers, process validation and registration of the biological product  * Lead and coordinate the global drug product sub-team (functional experts from e.g. formulation and process development, Analytics, Production, Device Development or Regulatory) * Be accountable for timely delivery of high quality source documents for submission, review of regulatory documents  * Setting priorities for the drug product sub-team  * Proactively communicate the overall project strategy and requirements, ensuring effective stakeholder engagement  * Assess and consolidate resource and project budget needs  * Strategically evaluate and integrate external assets for Drug Product Development (in-licensing, Mergers & Acquisitions (M&A)) in line with portfolio strategy    What you'll bring to the role: * Ph.D. in pharmaceutical technology, biotechnology, chemical engineering or equivalent  * Minimum of 8 years of relevant industry experience with a focus on drug product formulation and process development, technology transfers and regulatory submissions  * Proficient in quality principles, Quality by Design (QbD), Good Manufacturing Practice (GMP) and regulatory requirements with experience in Investigational New Drug (IND) / Biologics License Application (BLA) submissions  * Excellent leadership and interdisciplinary skills, with a track record of leading cross-functional global teams and projects  * Excellent project management, communication / presentation, stakeholder management and scientific / technical writing skills  * Openness to digital transformation and proactiveness in adopting new digital tools and Artificial Intelligence (AI)-driven solutions  * Strategic mindset with strong business acumen  * Fluency in English (oral and written)    You'll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards  In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is €78,383.90  /year (on a full-time basis). The actual salary will be significantly higher. https://www.novartis.com/careers/career-search/job/details/req-10065090-drug-product-project-leader-mfd-associate-director-science-technology https://www.novartis.com/careers/career-search/job/details/req-10065090-drug-product-project-leader-mfd-associate-director-science-technologyDivisionDevelopmentBusiness UnitInnovative MedicinesLocationAustriaSiteSchaftenauCompany / Legal EntityAT33 (FC...

1 Senior Expert Science & Technology - Data Science & Automation in Downstream Processing Job ID REQ-10065730 Location: Schaftenau, Austria  Role Purpose: Our Downstream Development team plays a crucial role in the late-phase development and transfer of biopharmaceutical drug substance (DS) processes. We are contributing significantly to bringing innovative biopharmaceutical drugs to the market and are dedicated to leveraging data science and automation to drive innovation and efficiency. We are currently seeking a highly skilled and motivated Senior Expert to join our dynamic DSP Development team focusing on data science and automation. In this role, you will be responsible for leading data science and automation projects as part of the portfolio pipeline projects in downstream process development. You will develop innovative solutions and support digital transformation initiatives. Your expertise will be crucial in supporting our data and digital initiatives, ensuring that our data strategies are aligned with our business goals.About the RoleKey Responsibilities: * Develop and evolve data and automation strategies for downstream process development activities * Collaborate with cross-functional teams to drive digital transformation and automation initiatives * Support and enhance data&digital and automation use cases by providing expert insights and solutions * Stay up to date with the latest trends and advancements in data science and automation technologies * Support and generating experimental data for process modeling in late-phase development, enabling targeted process characterization efforts * Evaluation of new technologies and equipment for automation of laboratory activities * Perform chromatography steps, cross flow filtration / tangential flow filtration and other membrane separation methods for purification of recombinant proteins as part of process development and characterization at laboratory and pilot scale * Independently plan, organize, perform and document scientific experiments; handle several activities at a time * Documentation of the studies in electronic documentation systems according to defined standards * Generate scientific documents to hand over to internal and / or external partners and support generation of international registration documents under minimal supervision. * Contribution to technology transfers to internal and external sites and definition of process steering controls Requirements: * Completed studies in Biotechnology, Process Engineering, Biology, Pharmaceutical Technology, Technical Chemistry, Pharmacy, Data Science or Computer Science (or comparable), ideally with several years of industry experience * Experience in data science, data engineering, and automation * Strong expertise in designing and optimizing data flows * Experience with data visualization tools and techniques * Experience in Downstream Processing, in particular with chromatography systems, e.g. ÄKTA systems * Proficiency in programming languages such as Python, R, or SQL * A personality with a can-do mentality and the ability to adopt to change with strong communication across organizational interfaces * Fluency in English In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is €65,605.54/year (on a full time basis). In most cases, the actual salary will be higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies. Apply to the job: https://www.novartis.com/careers/career-search/job/details/req-10065730-senior-expert-science-technology-data-science-automation-downstream-processing DivisionDevelopmentBusiness UnitInnovative MedicinesLocationAustriaSiteSchaftenauCompany / Legal EntityAT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH Das Mindestentgelt für die Stell...

YOUR FUTURE EMPLOYER From its foundation 185 years ago as a soap and candle start-up, P&G today is a leading consumer goods company. We are home to iconic, trusted brands that touch 5 billion consumers worldwide and make life a little bit easier in small but meaningful ways. We want you to bring your insight, creativity, and passion to join our dedicated teams who have helped us grow into a global company. Our people are our greatest asset: with our philosophy of promotion from within, ... 4 Internship in Engineering, Quality, Production and Material Process & Delivery (m/f/d) Our internship positions offer students the unique opportunity to test technical competence and management talent under real conditions and with specific tasks. A growing proportion of our junior staff are former interns. From Day 1, we want you to be part of our team which works on projects focused on inventing, reapplying and developing technologies required to support the production process of our extraordinary consumer products. Internship Positions are available in the following departments: * Engineering * Quality * Production * MPD (Material Process & Delivery) WHAT WE OFFER * 3-6 months projects with complex technical tasks, independence and rapidly growing personal responsibility in a young, dynamic team * Challenging projects to work on aimed at implementing new technologies, creating new concepts and improving our production processes * Possible stepping stone to a direct entry after graduation * Compensation: This position is subject to the Austrian Collective Bargaining Agreement for Employees in the Chemical Industry in employment group I. Job Qualifications * Minimum 3 completed semesters at the university * Targeted studies: Electrical / Mechanical / Process / Chemical / Industrial Engineering, Mechatronics, Automation Technology, Plastics Technology  * Very good analytical skills and quick comprehension * Creativity and problem solving skills * Above average academic performance * Extra-curricular activities * Good communication skills, assertiveness and teamwork * Good knowledge of English and German APPLICATION To optimally prepare for our online assessment & interviews, make sure you fully understand our http://www.pgcareers.com/global/en/hiring-process. Please ensure you provide: * CV as a separate document * Cover letter for the specific role you are applying for (optional) * Copy of high school certificate (Matura) as well as a copy of university degree diploma (if applicable) and enrollment confirmation as a university student Please upload all documents in the "CV/Resume" field. Incomplete applications may lead to delays in the recruitment process. At P&G #WESEEEQUAL We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click https://faq.pgwebtools.com/disability-accommodation-request/?fl_builder, if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience. Job Schedule - Full time Job Number - R000140927 Job Segmentation - Internships Apply Nowhttps://www.pgcareers.com/eu/en/job/R000140927/Internship-in-Engineering-Quality-Production-and-Material-Process-Delivery-m-f-d P&G Health Austria GmbH&Co. OG Hoesslgasse 20, 9800 Spittal an der Drau Tel: +43 4762 5151128 Mail: recruitingspittal.im@pg.com Das Mindestentgelt für die Stellen als Internship in Engineering, Quality, Production and Material Process & Delivery (m/f/d) beträgt 2.500,00 EUR brutto pro Monat auf Basis Vollzeitbeschäftigung. Bereitschaft zur Überzahlung.

YOUR FUTURE EMPLOYER From its foundation ... 2 Process Engineer - Spittal-an-der-Drau (m/f/d) YOUR ROLE as Process Engineer (m/f/d) As a Process Engineer, you will focus on optimizing production and / or packaging processes at our Plant in Spittal an der Drau. You will also be responsible for developing and implementing various projects. Your innovative ideas and contributions will significantly enhance the quality of our products. Your main tasks will include * Analysis and development of production processes * Development and implementation of production machines / system * Execution of product and plant tests * Improvement of existing production machines / automation processes * Planning, calculation and implementation of technical projects * Analysis and comparison of variants of technical development potential * Project Management * Growing personnel responsibility for the line teams Job Qualifications * Successfully completed degree in a technical field (e.g., mechanichal engineering, electrical engineering, process engineering) * Very good analytical skills and quick comprehension * Extra-curricular activities * Strong communication skills, assertiveness, teamwork and leadership skills * Initiative, flexibility and ability to coordinate * Good knowledge of English and German WHAT WE OFFER * Exciting work and responsibility from Day 1. * A permanent employment contract with a competitive salary, yearly performance-based compensation reviews, and a wide range of social benefits (e.g., flexible work environment, company pension plan, Christmas and vacation bonus, stock purchasing programs). * A customized personal development plan including relevant coaching, mentorship, training-on-the-job, and a large portfolio of individual technical upskilling opportunities * Diverse career perspectives * A vibrant international spirit with interactions on a regional/global level. * A dynamic and respectful environment - employees are at the core, we value every individual and support initiatives, promoting agility and life balance. * Compensation: This position is subject to the Austrian Collective Bargaining Agreement for Employees in the Chemical Industry in employment group IV. APPLICATION To optimally prepare for our online assessment & interviews, make sure you fully understand our http://www.pgcareers.com/global/en/hiring-process. Please ensure you provide: * CV as a separate document * Cover letter for the specific role you are applying for (optional) * Copy of high school certificate (Matura) as well as a copy of university degree diploma (if applicable) and enrollment confirmation as a university student Please upload all documents in the "CV/Resume" field. Incomplete applications may lead to delays in the recruitment process. At P&G #WESEEEQUAL We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click https://faq.pgwebtools.com/disability-accommodation-request/?fl_builder, if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience. Job Schedule - Full time Job Number - R000140928 Job Segmentation - Entry Level Apply Now https://www.pgcareers.com/eu/en/job/R000140928/Process-Engineer-Spittal-an-der-Drau-m-f-d P&G Health Austria GmbH & Co. OG Hösslgasse 20 9800 Spittal/Drau recruitingspittal.im@pg.com Das Mindestentgelt für die Stellen als Process Engineer - Spittal-an-der-Drau (m/f/d) beträgt 2.500,00 EUR brutto pro Monat auf Basis Vollzeitbeschäftigung. Bereitschaft zur Überzahlung.

YOUR FUTURE EMPLOYER From its foundation 185 years ago as a soap and candle start-up, P&G today is a leading consumer goods company. We are home to iconic, trusted brands that touch 5 billion consumers worldwide an... 2 Traineeship in Engineering, Quality, Production and Material Process & Delivery (m/f/d) Job Location: SPITTAL A.D. DRAU PLANT Job Description: Our traineeship positions offer students the unique opportunity to test technical competence and management talent under real conditions and with specific tasks. A growing proportion of our junior staff are former interns. From Day 1, we want you to be part of our team which works on projects focused on inventing, reapplying and developing technologies required to support the production process of our extraordinary consumer products. Possible projects Challenging projects to work on aimed at implementing new technologies, creating new concepts and improving our production processes. Some examples include * Development of innovative technologies around "continuous release" * Technical projects, e.g. developing new process, creative packaging solutions or new product models. * Sustainability studies around Packaging & Packaging Waste Regulation  WHAT WE OFFER * 9-12 months traineeship working on projects with complex technical tasks, independence and rapidly growing personal responsibility in a young, dynamic team * Activities together with other interns * Possible stepping stone to a direct entry after graduation * Compensation: This position is subject to the Austrian Collective Bargaining Agreement for Employees in the Chemical Industry in employment group I. Job Qualifications * Minimum 4-6 completed semesters in Science or Engineering disciplines * Targeted studies: Electrical / Mechanical / Process / Production / Industrial Engineering, Mechatronics, Automation Technology, Plastics Technology, Chemistry, Pharmacy, Physics * Very good analytical skills and quick comprehension * Creativity and problem solving skills * Above average academic performance * Extra-curricular activities * Good communication skills, assertiveness and teamwork * Good knowledge of English and German APPLICATION To optimally prepare for our online assessment & interviews, make sure you fully understand our http://www.pgcareers.com/global/en/hiring-process. Please ensure you provide: * CV as a separate document * Cover letter for the specific role you are applying for (optional) * Copy of high school certificate (Matura) as well as a copy of university degree diploma (if applicable) and enrollment confirmation as a university student Please upload all documents in the "CV/Resume" field. Incomplete applications may lead to delays in the recruitment process. At P&G #WESEEEQUAL We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click https://faq.pgwebtools.com/disability-accommodation-request/?fl_builder, if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience. Job Schedule - Full time Job Number - R000140923 Job Segmentation - Internships Apply Now https://www.pgcareers.com/eu/en/job/R000140923/Traineeship-in-Engineering-Quality-Production-and-Material-Process-Delivery-m-f-d P&G Health Austria GmbH&Co. OG Hoesslgasse 20, 9800 Spittal an der Drau Das Mindestentgelt für die Stellen als Traineeship in Engineering, Quality, Production and Material Process & Delivery (m/f/d) beträgt 2.500,00 EUR brutto pro Monat auf Basis Vollzeitbeschäftigung. Bereitschaft zur Überzahlung.

VOS MISSIONS * Assurer le maintien du statut validé de la base de données pour l'ensemble des vigilances * Développer et maintenir les différents modules de la base (matériovigilance et pharmacovigilance) * Mise en place et maintien d'un dictionnaire produit à jour dans la base pour les dispositifs médicaux ainsi que pour les médicaments. * Assurer la formation initiale et continue à la base selon les profils des collaborateurs impliqués dans la prise en charge des cas de vigilance * Amélioration continue des processus et activités liés à la base de données dont la gestion des fonctionnalités, des outils de requêtes, la gestion des Releases, des Mantis et des montées de version MedDRA et développer des indicateurs * Être la personne de contact pour toutes demandes relatives aux bases de données de vigilance et pour les problèmes identifiés sur la base de données, pour l'ouverture des tickets auprès du développeur et le suivi de la résolution des problèmes * Gérer les autres outils informatiques de suivi du pôle Case Management * Activités d'extraction de données à partir des systèmes d'enregistrement vigilance * Monitorer les demandes de requêtes pour la production des rapports de vigilance ou pour toutes autres types de demandes (questions des autorités, autorisation de mise sur le marché, audits et inspections, etc) * Gérer les activités liées à la cession/acquisition de produit/entité * Contribuer au maintien du User Guide notamment sur tous les aspects relatifs à la base de données * Bases de données Européennes : agir en tant que contact privilégier pour la base Eudravigilance (trust deputy Eudravigilance) ; Gérer les accès des collaborateurs vigilance impliqués dans l'extraction et gérer les aspects en lien avec la mise en production d'Eudamed (volet matériovigilance d'Eudravigilance). * Participer aux activités de data management * Effectuer et assurer la saisie des cas vigilance dans la base de données et participer au suivi de la compliance du pôle, dans le respect des délais requis par les réglementations et procédures en vigueur * Assurer l'anonymisation des document source et leur enregistrement dans la base de données * Contribuer à l'amélioration continue du contrôle qualité et des règles de saisie * Assurer les activités de suivi de la compliance du pôle (indicateurs de compliance et de performance) et contribution à la mise en place et au suivi de CAPA VOTRE PROFIL Formation : BAC+3 Expérience 2/3 ans sur un poste similaire Vos qualités personnelles : Rigueur, sens de l'organisation, réactivité et autonomie Bonne qualité relationnelle AUTRES INFORMATIONS Type de contrat : CDI Site de rattachement : Gentilly Prise de fonction souhaitée : dès que possible Avantages : I/P, tickets restaurant, participation aux frais de transport, œuvres sociales. Poste ouvert aux personnes en situation de handicap POURQUOI BIOCODEX : Nos quatre valeurs sont nos forces motrices et un ciment pour toutes les équipes : nous jouons collectif ; nous façonnons des relations justes ; nous osons innover ; nous prenons soin de notre écosystème. Convaincus que la diversité est source de richesse et qu'elle contribue de manière considérable à la pérennité de l'entreprise, nous traitons chaque individu de manière égale, indépendamment de son genre, de son âge, de son handicap, de sa nationalité ou de son orientation amoureuse. Chez Biocodex, notre démarche RSE holistique réconcilie les « 4P » : « People, Planet, Profit and Purpose » et nous souhaitons également fournir à l'ensemble de nos collaborateurs les ressources nécessaires pour leur réalisation professionnelle comme personnelle en leur offrant un large éventail d'avantages et de services compétitifs. Rejoignez-nous !

La ligne de service Consulting & Solutions d'Akkodis France renforce ses équipes en région normande et recrute un Ingénieur Qualification/Validation H/F en CDI à Rouen. Ce poste vous permet d'intervenir au sein d'une équipe dynamique dans le secteur pharmaceutique, sur des projets de qualification et validation d'équipements et procédés, en garantissant la conformité réglementaire et la fiabilité des processus industriels. Responsabilités principales : * Planifier et exécuter les activités de qualification et validation des équipements et procédés selon le plan directeur. * Rédiger, valider et revoir les protocoles et rapports de qualification/validation (IQ, OQ, PQ, QI, QO, FAT, SAT). * Assurer la conformité aux normes réglementaires pharmaceutiques et aux bonnes pratiques de fabrication (BPF, GMP). * Collaborer avec les équipes de production, qualité et maintenance pour garantir la fiabilité des processus. * Participer à l'analyse des écarts, émettre les fiches anomalies/déviations et proposer des actions correctives. * Gérer les documents techniques et assurer leur traçabilité via des logiciels de gestion documentaire. * Suivre les indicateurs de performance liés à la qualification et validation et contribuer à la formation des opérateurs. Environnement de travail : Vous rejoignez une équipe spécialisée dans le secteur pharmaceutique, impliquée sur des projets à forte exigence réglementaire. Vous interagissez étroitement avec les départements production, qualité et maintenance, et bénéficiez d'un environnement favorisant la gestion de projet, l'amélioration continue et l'accompagnement des collaborateurs. La méthodologie adoptée est centrée sur la rigueur documentaire, la traçabilité et l'application des standards internationaux. Profile Issu(e) d'une formation BAC+5 en ingénierie ou équivalent, vous disposez d'une première expérience réussie (3 à 5 ans) sur un poste similaire en industrie pharmaceutique ou dans un environnement réglementé. Vous maîtrisez les normes BPF, GMP et les méthodes de qualification/validation. Vous possédez des compétences avérées en rédaction technique, gestion documentaire, analyse de données et résolution de problèmes techniques. La connaissance des systèmes automatisés, du contrôle industriel et des outils informatiques est appréciée. Vous êtes autonome, rigoureux(se), organisé(e), et à l'aise dans le travail en équipe et la communication. Une bonne maîtrise de l'anglais technique est requise pour la documentation et les échanges internationaux. Akkodis accompagne ses clients dans la mondialisation de leurs projets, aussi un anglais courant est requis pour l'ensemble de nos collaborateurs.

En tant que Technicien Chimie Analytique, vos missions sont les suivantes : * Réaliser des analyses physico-chimiques pour le contrôle qualité et le développement analytique. Ces activités sont effectuées dans le respect du planning et des délais fixés, * Interpréter les résultats des analyses : transcrire les résultats, appliquer les méthodes de calcul spécifiées dans les procédures, interpréter les résultats et vérifier leur cohérence, * Participer aux investigations du laboratoire, * Signaler les non-conformités ou les déviations sur les produits et les équipements utilisés, les évaluer et proposer des solutions, * Participer aux vérifications de résultats internes au laboratoire, * Documenter rigoureusement l'ensemble de son activité, * Participer à l'optimisation de la gestion et de l'organisation du laboratoire, * Gérer les stocks de consommables et les déchets en cas de nécessité, * Remonter les dysfonctionnements et axes d'amélioration (documentation, manipulations.). De formation BTS en chimie minimum, vous justifiez d'au moins une première expérience en contrôle qualité analytique. Si vous ne répondez pas à l'ensemble de ces critères, n'hésitez pas néanmoins à nous transmettre votre candidature. Elle sera étudiée en toute confidentialité. * Intérim longue durée, * Salaire suivant expérience sur 12 mois, * Prime sur objectif, * Prime transport, * Ticket restaurant.