Valneva est une société spécialisée dans le développement et la commercialisation de vaccins prophylactiques contre des maladies infectieuses générant d’importants besoins médicaux. Le Groupe a mis à profit son expertise et ses infrastructures pour commercialiser avec succès deux vaccins et pour faire rapidement progresser un large éventail de candidats vaccins en développement clinique, et notamment ses candidats vaccins contre la maladie de Lyme, le virus du chikungunya et la COVID-19.

Valneva compte plus de 650 employés et exerce ses activités depuis l’Autriche, la Suède, la Grande-Bretagne, la France, le Canada et les États-Unis.

Nous recherchons deux Techniciens(nes) R&D Recherche Préclinique en CDD de 12 mois pour renforcer notre équipe basée à Saint-Herblain (Nantes).

Au sein de l’équipe Développement de procédés, vous assurerez les missions principales suivantes :

  • Mise en place et application de procédés de production des candidats vaccinaux en cours de développement en bioréacteur.
  • Mise en pratique des techniques telles que la culture cellulaire de mammifères, la transfection/l’infection de cellules eucaryotes et des méthodes analytiques couramment utilisés en virologie (SDS-PAGE, quantification par méthode biochimique, ELISA, test pour déterminer le titre viral).
  • Organisation et réalisation des expériences définies par le manager et les ingénieurs de l’équipe.
  • Proposition et réalisation de protocoles lors de la mise en place de nouvelles techniques ou en vue d’optimiser les techniques de routine.
  • Rédaction du cahier de laboratoire suivant les procédures appropriées : renseigner les séquences des expériences, les analyses des résultats et les observations scientifiques.
  • Rédaction des instructions, de protocoles et de rapports techniques pour assurer la transmission du savoir-faire.
  • Respect des normes d’assurance qualité et des règles d’hygiène, de sécurité, de confinement biologique et la confidentialité applicable à Valneva.
  • Contribution à l’entretien et au bon fonctionnement de l’équipement et du matériel de laboratoire.
  • Assurer la gestion des stocks de matériels et réactifs propres aux expériences en collaboration avec l’équipe Logistique.
  • Participation active à la vie de l’équipe.

Profil

  • Licence bio-industries, biotechnologies, ESTBA, ou autre formation avec dominante de culture cellulaire et développement de procédés de production en bioréacteur.
  • Trois années minimum d’expérience dans une entreprise de biotechnologie ou pharmaceutique.
  • Qualifié(e) dans le domaine de la biologie cellulaire et techniques biochimiques (compétences en virologie et biologie moléculaire sont un plus).
  • Autonomie dans l’organisation, la réalisation des expériences et l’analyse des résultats.
  • Maîtrise des logiciels (Word, Excel, Power Point).
  • Maîtrise de l’anglais indispensable : compréhension et expression écrite et orale.
  • Esprit d’équipe, flexible, curieux(se), attiré(e) par la découverte et les nouveaux défis.

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 650 employees.

Your responsibilities as Senior Scientist

  • Planning, analysis, review and troubleshooting of external pre-clinical animal models
  • Writing and reviewing of technical protocols / reports for external studies
  • Co-ordinate and liaise with external parties regarding pre-clinical animal models and other studies
  • Verification and review of set-up for immunological assays used for assessing pre-clinical vaccine candidates
  • Active participation at various vaccine programs or projects focusing on pre-clinical activities
  • Contribution to selection of new vaccine candidates for pre-clinical and clinical development
  • Build and maintain scientific expertise for dedicated vaccine indication
  • Become an integral part of highly interactive team working on multiple projects
  • Preparation and review of scientific manuscripts for publication

Your qualifications

  • PhD in relevant scientific field (preferred: immunology)
  • Several years of work experience in the life science environment
  • Background in vaccinology and animal models
  • Willingness to work in a research as well as GxP-regulated environment
  • Ability to work according to challenging timelines
  • Team work, excellent organizational skills
  • Excellent analytical/problem solving skills
  • Computer software (MS Office,…) and knowledge in statistical analyses
  • Fluent in English (oral and written), fluent in German

Our offer

  • Open, appreciative company culture with innovative spirit and attractive assignments
  • International surrounding with flat hierarchies
  • Good team spirit in a strong and highly motivated team
  • Wide range of benefits

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 48.000,- gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 650 employees.

Your responsibilities as Associate Clinical Strategy Manager

  • Provide medical writing for clinical and regulatory documents
  • Participate in development of clinical study documents and take over individual clinical study tasks after respective training
  • Support clinical study data analysis and interpretation of clinical trials
  • Organize advisory boards and study committees (Scientific Advisory Boards, DSMBs, Endpoint Adjudication Committees, etc.)
  • Conduct and summarize literature searches and competitive landscape reviews to support decisions on study designs, endpoints, assays, etc.

Your qualifications

  • PhD in Life Sciences, preferably in Pharmacy or Biology/Molecular Biology; applicants with a Master’s degree and relevant professional experience are also invited to apply
  • Ideally either thesis in an area related to clinical development, vaccines, infectious diseases or immunology, or initial professional experience with clinical development at a CRO or sponsor
  • Strong writing skills
  • Analytical and detail-oriented mind-set
  • Excellent command of English as the main working language
  • Self-organized work style
  • Scientific interest in clinical development of vaccines

Our offer

  • Open, appreciative company culture with innovative spirit and attractive assignments
  • International surrounding with flat hierarchies
  • Good team spirit in a strong and highly motivated team
  • Wide range of benefits like flexitime, performance-related bonus, lunch vouchers, child care center (“Kindergarten”), company events

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 45.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 650 employees.

Your responsibilities as Senior Clinical Strategy Manager

  • Execution of clinical development programs (currently especially Covid-19)
  • Provision of strategic development input and input to clinical development plans
  • Writing of individual study protocols
  • Drive data analysis and interpretation of clinical trials
  • Participation in the development of clinical study documents
  • Support of interactions with regulatory agencies and KOLs in therapeutic area of expertise

Your qualifications 

  • PhD in Life Sciences, preferably in Pharmacy or Biology/Molecular Biology; applicants with a Master’s degree and relevant professional experience are also invited to apply
  • Minimum of 5 years of professional work experience within clinical development (preferably in the Pharmaceutical/Biotech Industry)
  • Knowledge of GCP an relevant regulations
  • In-depth understanding of the drug development process
  • Strong writing skills
  • Strong presentation and communication kills
  • Ability to work in interdisciplinary teams
  • Project management skills
  • Analytical and detail-oriented mind-set
  • Excellent command of English as the main working language
  • Self-organized work style
  • Scientific interest in clinical development of vaccines

Our offer

  • Open, appreciative company culture with innovative spirit and attractive assignments
  • International surrounding with flat hierarchies
  • Good team spirit in a strong and highly motivated team
  • Wide range of benefits like flexitime, performance-related bonus, lunch vouchers, child care center (“Kindergarten”), company events

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 60.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical need. Valneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19.

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

We have a new opportunity within our Process Development team as Deputy Head of Department to support with our ongoing vaccine manufacturing in Livingston, Scotland.

Responsibilities

  • Ensure timely delivery of new vaccine products from development into clinical / commercial manufacture
  • Manage and lead delivery of new process introduction where identified for business required
  • Identify and manage delivery of process development / improvement projects, from conception to validation, with a view to increased process robustness, yield and success rate or reduced COGs to agreed timeframe
  • Ensure development Proposals, Plans and Reports are generated with adequately identified commercial considerations, impacts and milestones for delivery
  • Management of experienced scientists to ensure ownership and delivery of assigned project tasks, systems and areas of responsibility to agreed target dates
  • To deputise for the Head of Function or other departmental colleagues as required
  • Ensure consideration of risk and implementation of strategy
  • Ensure work plans are aligned with business requirements and site projects, goals & objectives
  • Deliver key critical data for the identification and mitigation of process risks or failure mechanisms through trending and escalation
  • Drive continuous process improvement and provide technical support to key site projects and business deliverables
  • Ensure the use of change management techniques and procedures for implementation where required.
  • Provide site wide technical expertise, key role in troubleshooting and lead key technical investigations / assessments, utilising critical trended data to support on time delivery of Quality Investigations
  • Support regulatory submissions by provision or review of technical reports and/or data
  • Manage and track on time delivery of department owned Quality Management System actions and documentation
  • Escalate deviations to compliance through senior site management
  • Represent the company to external contacts such as customers, suppliers and regulatory authorities for technical discussions
  • Ensure the required departmental training standards are maintained
  • Lead by example in the development and maintenance of an enthusiastic, supportive and collaborative environment within the team, across the site and between sites
  • Shift work and out of hours work as required
  • To undertake any other duties as requested by the line manager in accordance with company requirements

Experience

  • Degree qualification or equivalent experience in biological sciences or related discipline
  • Extensive experience of working within the Vaccine or Biologics Health Science sector, in Process Development, Manufacture or Analytical functions
  • Ideally experience of managing experienced Scientists
  • Strong GxP understanding and experience
  • Strong commercial awareness and demonstrable leadership
  • Good experience and understanding of protein chemistry and characterisation
  • Process / assay development experience of Biological systems, particularly viral products
  • Good experience of statistical data analysis and process trending
  • Experience of change management and risk analysis

Required Skills

  • Excellent communication and team management
  • Strong prioritisation capability in a fast paced environment with changing business priorities
  • Excellent Scientific understanding of vaccines or protein chemistry through development, manufacture or analytics
  • Concern for delivery
  • Analytical thinking
  • Team player with awareness of impact on people, process and systems

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical need. Valneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19.

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

We have a new opportunity within our Process Development team as a Senior Scientist to support with our ongoing vaccine manufacturing in Livingston, Scotland.

Responsibilities

  • Lead delivery of key tasks within the technical transfer and implementation programme for new IMP products into manufacture, including training and supervision in GMP production activities. Also for scale up from clinical to commercial manufacture. Ensure process robustness, consistency and yield
  • Lead delivery of key tasks within major development studies / projects, from concept to report. Consideration of risk and implementation strategy.
  • Lead delivery of key support tasks, e.g. development and production of new cell or viral bank processes / technologies, or newly defined operator qualification activities.
  • Support design & delivery of major process development / improvement projects, from conception to validation, with a view to increased process robustness, yield & success rate or reduced COGs to agreed timeframe.
  • Line management of department team members as required
  • Support preparation and delivery of production related tasks for commercialisation of IMP products, providing technical guidance to site
  • Key supervisor/operator and trainer for equipment and processes involved in GMP manufacture of viral vaccine product for clinical trial and process validation purposes.
  • Prepare Development Proposals, Plans and Reports, with identified costing, resources, and agreed milestones for delivery. Communicate plans effectively, with cross-functional consideration of site deliverables. Assist in troubleshooting and contribute to key technical investigations / assessments where required, to support on time delivery of Quality Investigations
  • Support regulatory submissions by contributing to provision of technical reports and/or data
  • Deliver assigned aspects of the Quality Management System and documentation to agreed timeframe. Escalate deviations in compliance to the Head of Department.
  • Participate in continuous process improvement and provide support to key site projects and business deliverables
  • Ensure training standards are maintained, as required in the role.
  • Actively contribute to the development and maintenance of and enthusiastic, supportive and collaborative environment within the team, across the site and between sites.
  • To deputise for the Process Development Principal Scientists, Deputy/Head of Department and team colleagues as required, and ensure owned tasks are assigned deputies in their absence
  • Shift work and out of hours work as required
  • To undertake any other duties as requested by the line manager in accordance with company requirements

Experience

  • Degree qualification in biological sciences or related discipline, or equivalent experience
  • Significant experience gained from several years within the Vaccine or Biologics Health Science sector or similar, in Process Development, Manufacture or Analytical functions
  • Several years experience of Biological process / assay development, scale up and optimisation
  • Cell culture experience/downstream processing/analytical techniques. Viral products beneficial
  • Proven ability to lead and deliver significant programmes of work
  • Strong experience/understanding of working in a GXP environment
  • Good experience/understanding in New Product Introduction / technology transfer for GXP Production

Required Skills

  • Excellent Scientific understanding of vaccines or protein chemistry through development, manufacture or analytics
  • Self-motivated, able to deliver to tight deadlines and pressure
  • Excellent communication and team management
  • Flexibility in dealing with challenging and rapidly changing priorities and workloads
  • Demonstrated creative & analytical thinking / problem solving skills
  • Consideration of impact and application of change on people, process and systems
  • Good organisational skills
  • Team player with awareness of impact on people, process and systems

Company Highlights
Valneva est une société spécialisée dans le développement et la commercialisation de vaccins prophylactiques contre des maladies infectieuses générant d’importants besoins médicaux. Valneva a une approche hautement spécialisée et ciblée du développement de vaccins en identifiant des maladies infectieuses mortelles et débilitantes pour lesquelles il n’existe pas de solution vaccinale prophylactique et pour lesquelles les options thérapeutiques sont limitées. Valneva utilise ensuite sa forte connaissance de la science des vaccins, et notamment son expertise dans les différents modes de vaccination ainsi que ses infrastructures de développement de vaccins déjà bien établies, pour mettre au point des vaccins prophylactiques destinés à lutter contre ces maladies. Le Groupe a mis à profit son expertise et ses infrastructures pour commercialiser avec succès deux vaccins et pour faire rapidement progresser un large éventail de candidats vaccins en développement clinique, et notamment ses candidats vaccins contre la maladie de Lyme, le virus du chikungunya et la COVID-19. Valneva compte environ 600 employés et exerce ses activités depuis l’Autriche, la Suède, la Grande-Bretagne, la France, le Canada et les Etats-Unis.

Key Responsibilities
Nous recherchons un(e) Technicien(ne) Logistique et Services Généraux en CDI pour renforcer notre équipe basée à Saint-Herblain (Nantes). Sous la direction du Responsable Achats Maintenance et Logistique France, vous assurerez les missions principales suivantes :

  • Assurer la réception des marchandises au quotidien :
    • Réception des marchandises livrées par les transporteurs incluant un contrôle visuel de l’état des colis.
    • Contrôle des marchandises réceptionnées : conformité des références livrées par apport aux commandes, respect des conditions de transport, intégrité des emballages.
    • Réception électronique des bons de livraison sous ERP (AX Dynamics).
  • Assurer la gestion des stocks et des références produits (sous ERP):
    • Gérer l’entrée en stock dans le magasin après réception.
    • Assurer la mise à jour quotidienne de l’état des stocks.
    • Créer les demandes d’achat nécessaires au maintien du stock.
    • Effectuer les sorties de stocks selon les procédures internes.
    • Créer les nouveaux articles non référencés.
  • Assurer les livraisons internes quotidiennes dans les laboratoires conformément aux bons de commande des opérateurs.
  • Assurer le suivi de prestataires externes : Gestion de l’arrivée et du départ des intervenants, accompagnement des prestataires dans le bâtiment et laboratoires.
  • Assurer le suivi de la prestation de bio-décontamination des laboratoires afin de suivre la bonne exécution des prestations demandées.
  • Assurer au quotidien les activités aux laboratoires :
    • Gestion des poubelles DASRI
    • Gestion de la laverie centrale
    • Gestion du rangement des sas et des laboratoires
    • Gestion des vêtements de travail de laboratoire (blouses et pyjamas)
  • Seconder le service de maintenance interne.
  • Réaliser des missions ponctuelles relatives au bon fonctionnement du bâtiment.

Profile
Formation Bac à Bac+2 en Logistique avec une expérience d’1 à 2 an(s).

  • Vous maîtrisez la saisie de demandes d’achat, de bons de livraison sous un logiciel de gestion de stocks et commandes (ERP).
  • Vous êtes rigoureux(se) et disposez d’excellentes qualités d’organisation.
  • Vous avez le sens du service client.
  • Vous êtes réactif(ve) et faites preuve d’initiative.
  • Vous êtes familier(e) du respect des procédures et instructions de travail.
  • Maîtrise de l’anglais indispensable.

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

Your responsibilities as Senior Technical Assistant – Quality Control

  • Execution of diverse analytical procedures (e.g. ELISA, HPLC, UV VIS spectrophotometry, cell based assays, etc.) for testing of release and stability samples for marketed products according to defined standard operating procedures and protocols in compliance with the same
  • Perform routine cell culture
  • Execute lab activities for set up, transfer and validation of assays required for the release of raw materials, intermediate products and final products, including preparation/completion of protocols and reports
  • Conduct on-time reporting according to the defined and trained document management standards including review and verification of analytical data
  • Preparation and review of GMP relevant documentation (e.g. Deviations, Changes, SOPs)
  • Active participation in laboratory investigations and documentation thereof (e.g. in case of Deviations)
  • Assume responsibility for laboratory equipment including qualification thereof and oversight of regular cleaning, calibration and maintenance

Your qualifications

  • Bachelor/Master Degree or equivalent level in a relevant scientific field
  • Excellent technical lab skills (immunological assays, cell culture, chemical / biochemical / bioanalytical methods)
  • Experience in cell culture and GxP environment
  • Experience with equipment qualification and method validation is a plus
  • Excellent organizational, documentation management and teamwork skills
  • Proactive, accurate, reliable working style and problem solving skills
  • Ability to work on competing projects with limited resources
  • Team work and excellent organizational skills

Our offer

  • Open, appreciative company culture with innovative spirit and attractive assignments
  • International surrounding with flat hierarchies
  • Good team spirit in a strong and highly motivated team
  • Wide range of benefits

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 40.000,- gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 650 employees. 

Your Responsibilities as (Senior) Technical Assistant – Clinical Trial Material Analytics

  • Setting up, transfer and validation of analytical GMP release and stability tests for multiple projects in the clinical development including preparation/completion of protocols and reports
  • Execution of diverse analytical procedures (e.g. ELISA, HPLC, cell based assays, etc.) as part of quality control testing of products / clinical trial materials according to defined standard operating procedures and protocols and in compliance with the same
  • Conduct on-time reporting according to the defined and trained document management standards including review and verification of analytical data
  • Preparation and review of GMP relevant documentation in English language (e.g. Deviations, Changes, SOPs)
  • Active participation in laboratory investigations and documentation thereof
  • Assume responsibility for laboratory equipment

Your Qualifications

  • MTA, BTA, DI (FH) or Master of Science in relevant field (Biology, Microbiology, Biotechnology, Bioengineering)
  • Experience working in a laboratory (preferably immunology, virology or biotechnology)
  • Working according to GxP within a recognized quality system is a plus
  • Experience working with cell based methods, ELISA, SDS-Page and/or HPLC is a plus
  • Experience working with the qualification and validation of product
    testing methods is a plus
  • Excellent organizational, documentation management and teamwork
    skills
  • Proactive, accurate, reliable working style and problem solving skills
  • Ability to work on multiple projects with challenging timelines

Our Offer

  • Open, appreciative company culture with innovative spirit and attractive assignments
  • International surrounding with flat hierarchies
  • Good team spirit in a strong and highly motivated team
  • Wide range of benefits

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 34.000,- gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

Valneva est une société spécialisée dans le développement et la commercialisation de vaccins prophylactiques contre des maladies infectieuses générant d’importants besoins médicaux. Valneva a une approche hautement spécialisée et ciblée du développement de vaccins en identifiant des maladies infectieuses mortelles et débilitantes pour lesquelles il n’existe pas de solution vaccinale prophylactique et pour lesquelles les options thérapeutiques sont limitées. Valneva utilise ensuite sa forte connaissance de la science des vaccins, et notamment son expertise dans les différents modes de vaccination ainsi que ses infrastructures de développement de vaccins déjà bien établies, pour mettre au point des vaccins prophylactiques destinés à lutter contre ces maladies. Le Groupe a mis à profit son expertise et ses infrastructures pour commercialiser avec succès deux vaccins et pour faire rapidement progresser un large éventail de candidats vaccins en développement clinique, et notamment ses candidats vaccins contre la maladie de Lyme, le virus du chikungunya et la COVID-19. Valneva compte environ 650 employés et exerce ses activités depuis l’Autriche, la Suède, la Grande-Bretagne, la France, le Canada et les Etats-Unis.

Key Responsibilities

Nous cherchons un(e) Technicien(ne) R&D Recherche Préclinique en CDI pour renforcer notre équipe basée à Saint-Herblain (Nantes). Sous la direction du Responsable Recherche Préclinique France, vous assurerez les missions principales suivantes :

  • Mise en place et application de procédés de production des candidats vaccinaux en cours de développement.
  • Mise en pratique des techniques telles que la culture cellulaire de mammifères, la transfection/l’infection de cellules eucaryotes et des méthodes analytiques couramment utilisés en virologie (SDS-PAGE, quantification par méthode biochimique, ELISA, test pour déterminer le titre viral).
  • Organisation et réalisation des expériences définies par le manager et les ingénieurs de l’équipe.
  • Proposition et réalisation de protocoles lors de la mise en place de nouvelles techniques ou en vue d’optimiser les techniques de routine.
  • Rédaction du cahier de laboratoire suivant les procédures appropriées : renseigner les séquences des expériences, les analyses des résultats et les observations scientifiques.
  • Rédaction des instructions, de protocoles et de rapports techniques pour assurer la transmission du savoir-faire.
  • Respect des normes d’assurance qualité et des règles d’hygiène, de sécurité, de confinement biologique et la confidentialité applicable à Valneva.
  • Contribution à l’entretien et au bon fonctionnement de l’équipement et du matériel de laboratoire.
  • Assurer la gestion des stocks de matériels et réactifs propres aux expériences en collaboration avec l’équipe Logistique.
  • Participation active à la vie de l’équipe.

Profile

  • Licence bio-industries, biotechnologies, ESTBA, ou autre formation avec dominante de culture cellulaire et développement de procédés de production.
  • Cinq années minimum d’expérience dans une entreprise de biotechnologie ou pharmaceutique.
  • Qualifié(e) dans le domaine de la biologie cellulaire et techniques biochimiques (compétences en virologie et biologie moléculaire sont un plus).
  • Autonomie dans l’organisation, la réalisation des expériences et l’analyse des résultats.
  • Maîtrise des logiciels (Word, Excel, Power Point).
  • Maîtrise de l’anglais indispensable : compréhension et expression écrite et orale.
  • Esprit d’équipe, flexible, curieux(se), attiré(e) par la découverte et les nouveaux défis