5 offres d'emploi
:

Île-de-France

  • Intitulé
  • Entreprise
  • Technicien d'Etudes VRD H/F

    • CDI
    • Seine-et-Marne (77)
    14/02/19
    Description de l'entreprise
    Page Personnel Immobilier Construction, partenaire privilégié du secteur du bâtiment et de la construction, recrute sur tous les maillons de la chaîne de construire (bâtiment, travaux publics, génie civil, infrastructures). Nos clients sont : Les entreprises générales, les bureaux d'études, les bureaux de contrôle, ainsi que les entreprises du second oeuvres (corps d'états techniques et architecturaux).
    Notre client est une entreprise nationale en plein développement, spécialisée dans le domaine de l'étanchéité, intervenant dans les secteurs des travaux publics et du génie civil.
    Description du poste
    En tant que Technicien d'Etudes VRD et rattaché au Responsable d'Etudes, vous prenez en charge plusieurs projets de VRD et GC. Vos principales missions sont les suivantes :
    Pour les études de prix :
    * Analyser les dossiers ;
    * Réaliser les métrés et les mesures sur le terrain ;
    * Lancer et analyser les consultations auprès des fournisseurs ;
    * Rédiger les mémoires techniques.

    Pour les études techniques en exécution :
    * Réaliser les calculs topographiques ;
    * Participer à la préparation des chantiers en cours (plans d'exécution et documents de suivi qualité),
    * Établir les plans d'implantations ;
    * Établir les dossiers de recollement.

    Cette liste de tâches n'est pas limitative. Une formation interne et un accompagnement aux procédures et méthodes de travail sont également mises en place par la structure lors de votre arrivée.
    Description du profil
    Titulaire d'un Bac +2 minimum (BTS Économie de la construction ou TP, DUT GC...), vous disposez d'au moins une expérience comme Technicien d'Etudes VRD ou Dessinateur-Projeteur VRD, au sein d'une entreprise de travaux publics ou au sein d'un bureau d'études.
    La maîtrise du logiciel AutoCAD est attendue à ce poste.
    Une connaissance de Covadis est un plus.
    Méthodique et ordonné, votre capacité à communiquer et votre sens de l'écoute sont indispensables pour mener à bien votre mission.

    Conditions et Avantages

    Le poste est basé en Seine-et-Marne.
  • Software QA Engineer - Ingénieur Qualité Logiciel (H/F)

    • CDI
    • Île-de-France • Villejuif (94) - Île-de-France
    04/02/19
    Description de l'entreprise

    Who we are?

     

    Stilla Technologies (http://www.stillatechnologies.com) is a Paris-based “tools for Life Sciences” company that helps scientists build the future of medicine.

     

    Since 2016, Stilla Technologies has been providing research organizations specialized in molecular biology and genetic analysis with its Naica™ System, a ground-breaking digital PCR solution that enables scientists to detect and quantify DNA mutations with unrivalled precision.

     

    With the Naica System, researchers worldwide are developing a new generation of high-precision genetic tests, in various fields of applications such as liquid biopsy tests for cancer diagnostics and non-invasive prenatal testing, as well as GMO detection.

     

    After closing a 16 M€ Series A funding round in November 2018, Stilla is scaling its operations worldwide, with a focus on maintaining a strong R&D pipeline of innovative products for precision genetic analysis (instrumentation, software, consumables and assays).

     

    Stilla’s talented and multidisciplinary team shares a passion for building successful Life Science products based on deep technological innovations. We are pursuing a huge potential market and aim to become the new leader in the exciting field of precision genetic analysis.

     

    Join us!

    Description du poste

    Stilla is hiring a Software QA (Quality Assurance) Engineer whose main missions will be to maintain and improve automated software test development, participate to continuous integration and version management, and document software product validation.

     

    Missions for the Software QA Engineer

     

    The Software QA Engineer will be in charge of the following missions:

     

    1. Maintain the current software tests, and write new ones (when applicable: unit tests, integration tests, user tests, risk mitigation tests)

      • Work together with the software developers to ensure that each incoming feature comes along with a nice set of tests
      • Understand the user needs and scenarios to create relevant tests with suitable evaluation criteria
      • Maintain and improve test coverage

    2. Provide up-to-date software documentation, including software architecture design, technical specifications, test plans and test reports

    3. Perform regular code review and propose appropriate improvements or corrections

    4. Contribute to the most user-friendly and stable software in Life Science

    5. Perform regular technological intelligence and propose innovative solutions

    6. Punctually contribute to software customer support, when needed

    7. Get involved in a software dream team in the company
    Description du profil

    Our ideal candidate:

     

    • Has minimum 2-3 years of experience in software quality assurance
    • Feels responsible for software code quality, readability and durability (especially in C++)

    • Has ideally a first experience of the Qt / Squish environment along with basic Visual Studio and C++ projects, and additional experience in Python / JavaScript & SQL programming

    • Combines agile software development with continuous integration (using these tools or equivalent ones: Git, Redmine, Jenkins)

    • Has ideally some experience in software risk analysis and software lifecycle management (IEC 62304, IEC 62366, 21 CFR Part 11 standards)

    • Must be fluent in French and technical English

    • Enjoys team working and knowledge sharing in a multidisciplinary environment (experts in software development but also in microfluidics, molecular biology, micromechanics, marketing & business development, etc.)

    • May not know what digital PCR is about but is very curious about it…

    • Is motivated by ambitious objectives and willing to bring significant contributions to science and medicine!
  • Experienced C++/Qt Software Developer - Développeur...

    • CDI
    • Île-de-France • Villejuif (94) - Île-de-France
    04/02/19
    Description de l'entreprise

    Who we are?

     

    Stilla Technologies (http://www.stillatechnologies.com) is a Paris-based “tools for Life Sciences” company that helps scientists build the future of medicine.

     

    Since 2016, Stilla Technologies has been providing research organizations specialized in molecular biology and genetic analysis with its Naica™ System, a ground-breaking digital PCR solution that enables scientists to detect and quantify DNA mutations with unrivalled precision.

     

    With the Naica System, researchers worldwide are developing a new generation of high-precision genetic tests, in various fields of applications such as liquid biopsy tests for cancer diagnostics and non-invasive prenatal testing, as well as GMO detection.

     

    After closing a 16 M€ Series A funding round in November 2018, Stilla is scaling its operations worldwide, with a focus on maintaining a strong R&D pipeline of innovative products for precision genetic analysis (instrumentation, software, consumables and assays).

     

    Stilla’s talented and multidisciplinary team shares a passion for building successful Life Science products based on deep technological innovations. We are pursuing a huge potential market and aim to become the new leader in the exciting field of precision genetic analysis.

     

    Join us!

    Description du poste

    Stilla is hiring an Experienced C++/Qt Software Developer whose main missions will be to build efficient, innovative and sustainable software products, contribute to existing ones and lead new software research and development projects

     

    Missions for the Experienced C++/Qt Software Developer

     

    The Experienced Software Developer will be in charge of the following missions:

     

    1. Conceive and develop new software features / new software products from functional specifications brought by need analysis

    2. Ensure the sustainability of the developed software components, for both internal and external products

    3. Contribute to the documentation of software technical specifications and software component evaluation

    4. Perform regular technological intelligence and propose innovative solutions

    5. Punctually contribute to software customer support, when needed

    6. Get involved in a software dream team in the company
    Description du profil

    Our ideal candidate:

     

    • Has 3 minimum years of experience in industrial software development, if possible in a cross-platform environment (Windows, Linux) and covering low-level to high-level software development

    • Masters sustainable C++ programming (design patterns, test-driven development, latest standards up to C++17) and is familiar with the Qt Framework

    • Has ideally a significant experience in embedded software development

    • Combines agile software development with continuous integration (using these tools or equivalent ones: Visual Studio, CMake, Git, Redmine, Jenkins)
    • Is familiar with the use of open-source libraries compatible with commercial exploitation

    • Has experience in software project management, including planning follow-up and documentation of technical specifications

    • Has ideally additional experience in some of these domains: Python / JavaScript / SQL programming; image processing / computer vision algorithms; applied statistics / bioinformatics; IEC 62304 and 21 CFR Part 11 standards

    • Must be fluent in French and technical English

    • Enjoys team working and knowledge sharing in a multidisciplinary environment (experts in software development but also in microfluidics, molecular biology, micromechanics, marketing & business development, etc.)

    • May not know what digital PCR is about but is very curious about it…

    • Is motivated by ambitious objectives and willing to bring significant contributions to science and medicine!
  • Responsable Administration des Ventes

    • CDI
    • Les Ulis (91) - Île-de-France
    28/01/19
    Description de l'entreprise

    Au service du développement économique et des territoires, la CCI Essonne se mobilise au quotidien afin que les entreprises puissent se développer, investir, innover, gagner des marchés et créer de l'emploi. Pour cela, elle met à disposition de l'information, de l'expertise, du conseil et des accompagnements...

    Description du poste

    La CCI Essonne recherche un Responsable Administration des Ventes (H/F) pour accompagner le développement d’une PME spécialisée depuis 1983 dans la fabrication de dispositifs de Diagnostic In Vitro utilisés par les laboratoires de Biologie Médicale.

     

    Basée à Courtaboeuf la société, au chiffre d’affaires en constante progression, fabrique et distribue des produits de Diagnostic In Vitro de haute qualité pour répondre aux exigences de ses clients.

     

    Sous la responsabilité du Directeur des ventes, le Responsable Administration des Ventes aura en charge :

    • La gestion des marchandises,
    • La participation aux réponses aux appels d’offres,
    • Le suivi des livraisons clients,
    • La facturation,
    • La gestion des outils statistiques relatifs aux achats/ventes,
    • La veille des outils de gestion (SAGE, Open Bee).
    Description du profil

    Maîtrise de l’anglais et des outils informatiques (Sage, TNT …).

    La rigueur, l’organisation et la réactivité alliées à un esprit d’équipe sont les aptitudes nécessaires à la réussite de ce poste.

  • Directeur / Directrice des Opérations

    • CDI
    • Villejuif (94) - Île-de-France
    21/12/18
    Description de l'entreprise

    Stilla Technologies est une start-up Européenne pionnière dans le domaine de l’instrumentation pour la recherche en biologie, qui a pour objectif d’aider les chercheurs à développer les tests génétiques de demain.

    Depuis 5 ans, notre équipe d’ingénieurs et scientifiques développe un instrument d’analyse génétique de nouvelle génération, appelé le système Naica(TM).

    S’appuyant sur une technique innovante développée à l’Ecole Polytechnique, ce système permet aux laboratoires de recherche de détecter et quantifier des mutations génétiques avec une précision inégalée ! Les chercheurs utilisent le Naica pour construire les tests génétiques de demain qui permettront de suivre l’évolution de cancers directement à partir de prises de sang, détecter les traces du VIH pour savoir si le patient est totalement guéri, quantifier la présence d’OGM dans les aliments etc…

    Depuis le lancement commercial du système en 2016, nous triplons notre chiffre d’affaires chaque année. En octobre 2018, nous avons bouclé un tour de financement de 16 M€ avec des fonds d’investissements de référence pour accélérer notre croissance à l’international et développer notre nouvelle gamme de produits !

    Description du poste

    After closing a 16 M€ Series A funding round in November 2018, Stilla is scaling its operations worldwide, with a focus on scaling and de-risking the company’s operations.

    Stilla is hiring a VP of Operations whose main missions will be to scale-up and de-risk the company’s operations (supply chain, production, logistics…).

     

    Missions for the VP of Operations

    The VP of Operations oversees Production, Logistics and Maintenance. He/She coordinates with Sales for planning the deliveries and installs, with Quality to set up and drive continuous improvement programs and ensure compliance to standards, with Support to plan for returns and repairs, and with R&D for the launch of new products. The VP of Operations reports directly to the CEO and manages the Operations financials.

    1. Ramp up production according to Stilla’s business plan

    • Grow production capacity
    • Coordinate with Sales for planning management
    • Coordinate with R&D for the production start of new products
    • Drive standardization and automatization of Operations
    • Drive the commissioning of new manufacturing facilities
    • Coordinate with Support for returns and repairs and for Warranty management

     

    2. Derisk all aspects of Operations at Stilla

    • Identify, prioritize and address all risks related to Operations (technical-wise, supplier-wise …)
    • Negotiate partnerships and supply agreements with key suppliers
    • Monitor and report the progress of derisking
    • Solve identified risks

     

    3. Manage the financials of Operations

    • Monitor the costs of Operations through ERP logs (Purchasing, Manufacturing, Stock value, Transport, VAT …)
    • Define and report KPIs for Operations (COGS, Failure rates …)
    • Manage the budget of the Operations department

     

    4. Grow a team of specialists

    • Hire Production, Maintenance and Logistics specialists
    • Organize and Lead Operations in specialized teams (Production, Maintenance and Logistics)
    • Roll out trainings for specialists

     

    5. Make all processes of Operations IVD compliant

    • Coordinate with Quality and R&D for IVD compliance
    • Put in place key processes for IVD compliance (Consumables, Instruments, Assays)

     

    Stilla’s talented and multidisciplinary team shares a passion for building successful Life Science products based on deep technological innovations. We are pursuing a huge potential market and aim to become the new leader in the exciting field of precision genetic analysis. Join us!

     

    Description du profil

    Our ideal candidate

    • Has one or more successful experiences ramping up production volumes for instrumentation and consumable products
    • Has successful experience negotiating contracts with key suppliers
    • Has 10+ years of experience in a relevant industry
    • Has experience managing and coordinate teams
    • Must speak French and English fluently

     

    Why join us?

    • Build large scale Operations in a challenging environment!
    • Join a young and dynamic Life Science company growing at a 3-digit pace!
    • Work with a team who shares a passion for building successful Life Science Products based on deep technological innovations.