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Testing Technician

Job BriefThis role performs engineering technician duties, product testing and related project support functions at the Yamaha Marine Test Facility with the purpose of improving current Yamaha Marine products and developing innovative new marine products.Yamaha has an excellent opportunity for a Testing Technician to join our Marine team in Bridgeport, AL. This role performs engineering technician duties, product testing and related project support functions at the Yamaha Marine Test Facility with the purpose of improving current Yamaha Marine products and developing innovative new marine products. Specific duties include, but are not limited to:Install outboard engines, control systems, electronics and marine accessories on a wide variety of applications.Operate a wide variety of boat applications in varying conditions while collecting performance data and engine diagnostic information.Apply advanced knowledge of marine products and technology as well as basic practical machining skills in order to make modifications to engines and other marine products for the purpose of collecting research and development data.Apply marine combustion engine theory and marine propulsion system theory and knowledge in order to effectively service, maintain and diagnose marine engines, engine accessories.Apply marine ac/dc electrical theory as well as knowledge of CAN systems to maintain and diagnose issue with marine boat control systems, marine electronics and a wide variety of boat accessories.Install advanced diagnostic and data collection tools and equipment for the purpose of acquiring, analyzing, and reporting marine product performance data and information using Microsoft office and other computer applications.Under minimum supervision, create and execute test plans according to strict industry standards and guidelines set by marine manufactures and related industry organizations. Maintain a safe and clean environment within all areas of the buildings, grounds and docks. Assist in performing routine repairs and maintenance on company equipment, vehicles, buildings, docks and grounds.Complete confidentiality is mandatory on testing activities, results and products.Assist in planning and participate in field testing, market research, and market service issue investigation. Qualifications:High School Diploma and some college preferred with excellent skills in math and science.Completion of state specific boating safety course.Must have at least 5 years’ experience in boat, engine and electronics rigging, repair and maintenance.Major OEM service certifications are very beneficial.CDL is BeneficialAbility to analyze and resolve problems encountered in testing or with equipmentProficient in computer programs such as Excel, Word, Adobe, and Power Point.Must have experience operating a forklift, trucks, and towing trailers.Requires close attention to detail regarding engineering data and project results.Requires up to 15% travelMust observe all safety rules and regulations. Safe operation of all equipment.

Yamaha Motor Co. USA • Bridgeport, U.S.

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REMOTE - Mobile Apps DevOps Engineer

Remote - Mobile Apps CI/CD DevOps Engineer - 12 months+ contract - W2 submissions only (no third party/ C2C submissions allowed)Seeking a talented DevOps Engineer Ld with mobile application experience to join our Infrastructure Services Team for the Mobile Native Apps platform.Role: This DevOps Engineer will be maintaining, architecting, and implementing our continuous integration pipeline to drive the development and automated testing of mobile iOS and Android applications.Will have the opportunity to work with a group of top-notch mobile software and test engineers. To be successful in this role, the candidate must be hands-on, proactive, good at problem solving, and have a strong desire to learn and drive for results.Duties will primarily be improving software delivery practices around continuous integration and testing of code.Developing build, test and deployment scripts and designing infrastructure and application configurations for continuous integration and delivery.In addition, responsible for monitoring and reporting on the health of the CI/CD pipelines and seeking out ways to continuously improve the performance of them and the productivity of 9 scrum teams.As part of the Enterprise Monitoring Team, help to deliver best in class monitoring capabilities and services to improve the maturity of performance, availability, and capacity management processes for both the applications and infrastructure components.As an Agile delivery team member, provide customers with the near real time observability needed to rapidly respond to events, while advancing the client's monitoring capabilities. Assist in evaluating, designing, and implementing software products to support customer requirements, as well as perform research and development efforts pertaining to new features and capabilities.Required skills:* 2+ years of experience with mobile apps (iOS and Android) build systems & deployment.* Experience with industry CI/CD tools (e.g., Azure DevOps, Teamcity, Buildkite, Bitrise, Github Actions, CircleCI, etc.).* Experience with cloud build agents for Mac (e.g., AWS EC2, Mac in Cloud, etc.) is a plus.* Knowledge of package and configuration management tools (Terraform, Puppet, Ansible, etc.) and containers such as Docker (compose, private registries).Preferred skills and experiences:* Experience with package distribution systems (Nexus, Artifactory, etc.)* Proficient with at least one scripting language (Bash, Python, Shell, etc.)* Solid experience with packaging components (Cocoapods/Jar) and distributing them to internal and external customers* Strong understanding of Git development workflows and branchingDay-to-Day Responsibilities:* Maintain and enhance our Android and iOS CI/CD build and release orchestration scripts and tools. Current stack:o Azure Dev Ops (ADO).o Automated testing tools (Espresso, KIF).o Fastlane and Gradle.* Research and recommend improvements for static analysis solutions for linting, accessibility, performance, security, etc. to improve CI/CD capabilities.* Automate manual processes in our build, test, and release stages.* Own tooling roadmaps to introduce new tools and take advantage of new features for current tools.* Monitor build times to ensure they stay within established ranges.* Participate in coordination and release of production deployments.

Careerbuilder • Cleveland, U.S.

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Agronomy / Horticulture Senior Research Technician

South Dakota State UniversityPhysical Location of Position (City): Beresford (SD)Posting TextJob Responsibilities: This position will work with diverse research projects at the SDSU Southeast Research Farm in Beresford, SD. The primary focus will be on cropping systems research with both agronomic and horticultural crops at the farm; to engage with livestock and other farm research and maintenance efforts as directed by the Operations Manager; implement assigned trials, including collecting and storing samples, recording data, and providing for field and plot maintenance, and equipment as directed and based on protocols provided by SDSU researchers; summarize data collected and transmit it to project directors, and assist with analysis and interpretation of data; help prepare presentations and reports in coordination with the project director and the operations manager of the farm. Knowledge, Skills & Abilities:Knowledge of:Commercial crop or vegetable productionFarm equipment operation and maintenanceAgronomic or horticultural researchData management and software for controlling precision ag equipmentSkill & Ability to:Demonstrate ability to work with famers and other clientele groupsWork in the field and to travel as needed to complete assigned tasksBe self-motivated, disciplined, and ale to understand and adhere to research protocolsWork independently on a day-to-day basisRequired License: Valid driver’s license. Commercial pesticide applicator license within 6 months of hire.

Glassdoor Inc. • Brookings, U.S.

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Ingénieur Applicatif C/C++ (H/F)

Poste & MissionsSous la responsabilité d’un chef de produit, vous intégrez la cellule R&D composée de 15 personnes. A ce titre, vos missions sont les suivantes :• Participation au design de l’application, et aux évolutions techniques et fonctionnelles • Définition de l’architecture technique • Test automatiques • Développement de nouvelles fonctionnalités en C++ • Documentation de votre code • Support et accompagnement de vos clients • Participation à la stratégie produitProfilVous êtes diplômé d’un Bac+5 en informatique, et avez une première expérience significative en développement C++.Vous maîtrisez les langages et environnements suivants : • C/C++ • Excellentes connaissances sur Windows/Linux • La connaissance de Javascript/ NodeJS est un plus • Idéalement, vous avez déjà travaillé dans le domaine de la cybersécurité. Si non, vous êtes très intéressé par ce secteur d’activité ! Vous avez un niveau d’anglais, vous permettant de lire, comprendre, et de rédiger de la documentation technique. Votre rigueur alliée à votre adaptabilité et votre sens d’organisation font de vous le candidat idéal pour ce poste. Votre sens du service et votre curiosité vous permettront de mener à bien les missions qui vous sont confiées. Vous vous êtes reconnu dans ce descriptif ? Vous avez envie de vous investir et d’évoluer au sein d’une société en pleine expansion ?

Approach People Recruitment • Lyon, France

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Ingénieur projets – Medical devices

Vos Missions :• Rédiger et exécuter des protocoles d’essais en respectant les standards internes. • Définir et participer aux étapes d’industrialisation et / ou amelioration de procedés de fabrication • Définir la stratégie et exécuter les validations initiales des nouveaux procédés et équipements complexes • Participer au transfert technologique des procédés de fabrication définis et communiqués par les équipes Développement et projets, • Créer ou mettre à jour la documentation projet ou du système du SMQ dans le cadre de son activité en conformités avec les standards internes. • Soutenir les activités de production en prodiguant une expertise pour la résolution de difficultés process Proposer, harmoniser et implémenter les méthodes de travail en vue de cette amélioration • Participer et/ou animer le processus d’analyse de risque, • Participer si nécessaire au processus de déviation, investigation et CAPA • Participation aux validations ou revues périodiques, • Réaliser un reporting régulier de son activité, • Veiller au respect du système Qualité en vigueur, des bonnes pratiques de fabrication, des règles d’hygiène et de sécurité, des règles de fonctionnement de l’entreprise. • Préparer la documentation technique nécessaire pour soutenir un examen des autorités compétentes concernées, en accord avec les normes applicables en vigueurQualifications & Experience• Diplôme d’ingénieur ou équivalent, • Expérience d’au moins 2 ans en R&D ou en Engineering, idéalement acquise dans le domaine de la chimie des polymères, des dispositifs médicaux. en qualification / validation • Connaissances de la norme ISO13485, des BPF et autres normes applicables au dispositif médicaux • Maîtrise des outils informatiques de bureautique standards • Français et anglais courant • Expérience projet en tant qu’acteur ou gestionnaire ayant permis de démontrer une aisance relationnelle, des capacités à dialoguer avec des interlocuteurs variés internes et externes à l’entreprise

Approach People Recruitment • Lausanne, Switzerland

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Designer, Color, Materials, & Trend

Designer, Color, Materials, & TrendYou'll be a trusted member of our team reporting to the Color, Materials & Trend team within the global Footwear Design function (Men’s, Women’s, Street, Outdoor). As the Designer, Color, Materials & Trend, you will execute the seasonal creative direction through color and material design application. You will realize trend-relevant, narrative-driven concepts with color, materials, graphics and details that support the seasonal brand strategy and storytelling across Footwear Design. Bring your purpose and curiosity to this role in order to drive newness, energy and move the brand forward. How You Will Make a Difference What you will do:Apply color and material direction to footwear designs across categories based on seasonal creative directionSupport the Color/Trend/Materials Design team through research and development of color and material trends Collaborate with Design team to understand category and color flow based on seasonal direction, color strategy and storytellingCreate seasonal graphic and print designsProvide color design support for design team as needed outside of assigned product loadMaintain CAD files in company Product Line Management (PLM) systemResearch color and style trend analysis and communicate to the product development team via samples, trend boards, etc.As the Designer, Color/Materials/Trend, you will be responsible for executing the seasonal Creative Direction through color and material design application. You will realize trend-relevant, narrative-driven concepts with color, materials, graphics and details that support the seasonal brand strategy and storytelling across Footwear Design. Bring your purpose and curiosity to this role in order to drive newness, energy and move the brand forward.Skills for SuccessYears of Related Professional Experience: 3-5 experience or 2+ years of related experience and trainingEducational Position Requirements: A formal education and subsequent undergraduate/graduate degrees such as a bachelor’s degree or equivalent from a four-year collect industrial or fashion/textile design or graphic design are nice to have, we are most interested in your total experience and professional achievements.What we expect you already know/have:A strong understanding of color theory and visual acumenA strong understanding of leather and textilesThe ability to influence and collaborate with key business partners and stakeholdersThe ability to manage multiple projects at once and meet seasonal milestones and key deadlinesExperience in footwear or apparel design or an equivalent combination of technical experience and trainingProficiency with computer design software, i.e., Adobe Illustrator, Adobe Photoshop)Proficiency with business computer software, i.e., Microsoft Excel, Work, PowerPoint, Apple KeynoteKnowledge of additional computer design (Solidworks, Alias, Rhino or other design software) is a plusProfessional presentation skillsThe ability to ready, analyze and interpret product design briefsThe ability to establish and maintain effective relationships with cross-functional partnersExcellent interpersonal and communication skillsExcellent problem-solving skillsThe ability to travel internationally and domestically as needed (10-20 percent of the time)The willingness and ability to work additional hours as neededThe ability to bend, lift, open and move product and related office items varying in weight from 1-25 pounds, depending on the need

Timberland Company • Portsmouth, u.s.

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Ingénieur projets – Dispositifs médicaux

Description de l'offreNotre client, leader mondial dans le domaine des dispositifs médicaux, est actuellement à la recherche d’un(e) ingénieur projet.Description du poste :Rédiger et exécuter des protocoles d’essais en respectant les standards internes.Définir et participer aux étapes d’industrialisation et / ou amélioration de procédés de fabricationDéfinir la stratégie et exécuter les validations initiales des nouveaux procédés et équipements complexesParticiper au transfert technologique des procédés de fabrication définis et communiqués par les équipes Développement et projets,Créer ou mettre à jour la documentation projet ou du SMQ dans le cadre de son activité en conformités avec les standards internes.Soutenir les activités de production en prodiguant une expertise pour la résolution de difficultés process.Proposer, harmoniser et implémenter les méthodes de travail en vue de cette amélioration.Participer et/ou animer le processus d’analyse de risque,Participer si nécessaire au processus de déviation, investigation et CAPAParticipation aux validations ou revues périodiques,Réaliser un reporting régulier de son activité,Veiller au respect du système Qualité en vigueur, des bonnes pratiques de fabrication, des règles d’hygiène et de sécurité, des règles de fonctionnement de l’entreprise.Préparer la documentation technique nécessaire pour soutenir un examen des autorités compétentes concernées, en accord avec les normes applicables en vigueurLe profil :Diplôme d’ingénieur ou équivalent,Expérience d’au moins 2 ans en R&D ou en Engineering, idéalement acquise dans le domaine de la chimie des polymères, des dispositifs médicaux, en qualification / validationConnaissances de la norme ISO13485, des BPF et autres normes applicables au dispositif médicauxMaîtrise des outils informatiques de bureautique standardsFrançais et anglais courantExpérience projet en tant qu’acteur ou gestionnaire ayant permis de démontrer une aisance relationnelle, des capacités à dialoguer avec des interlocuteurs variés internes et externes à l’entreprise

Approach People Recruitment • Lausanne, Suisse

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Ingénieur développement H/F

Job DescriptionUn éditeur de logiciel dans le secteur des télécommunications, leader mondial sur le marché du radio planning et de l’optimisation des réseaux de téléphonie mobile avec 10 000 licences à travers 140 pays.Au sein de l’équipe de développement et après une période de formation sur le logiciel, vous participez au support de clients internationaux !Vous développez le logiciel et êtes en contact direct avec les clients utilisateurs internationaux pour les accompagner dans leurs développements sur le logiciel Vos principales responsabilités :Accompagner les clients et distributeurs dans leurs développements sur le logicielSupport technique des clients et des distributeurs internationaux par téléphone et par email : Prise en charge et résolution.Travailler en étroite collaboration avec les équipes de développement pour anticiper les nouvelles évolutions produit.Être le lien entre les clients et les équipes internesRéalisation de développement en Python et Javascript (Angular)Echanges quotidiens en anglais dans un contexte international Environnement technique :Pyhton / Javascript / AngularREST & COM API’sMicrosoft visual studio code / GIT / Swagger / PostmanDocker, SwarmBases de données : Oracle, SQL Server, PostgreSQL, MongoDBCloud : AWS, GCP, AzureProfil :Vous êtes titulaire d’un Bac+5 ingénieur spécialité informatiqueVous avez une première expérience significative en développement Python – FullstackDéveloppement Web, JSON, XML, SQLVotre Anglais est courantBon communiquant, aisance relationnelle

Approach People Recruitment • Toulouse, France

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Research Associate

A Pharmaceutical Company is seeking a Research Associate in Frederick, MD. Role Description This role will provide process engineering and analytical support for commercial manufacturing of cell therapy. Working cross functionally with quality, operations, material management, facility and engineering functions, the role is expected to provide technical input for product/process response and investigations, technology implementation, technology transfers, process validation and regulatory filings. • Execute scientific laboratory studies to support process/product understanding and continuous improvement projects • Execute analytical testing of cell therapy products – flow cytometry, ELISA and PCR assays. • Ability to follow laboratory procedures with attention to detail, and successfully execute experiments at the bench • Provide technical input to the execution of process validation and comparability campaigns. • Participate in evaluation of new technology and process automation for introduction into GMP manufacturing • Participate and support process FMEAs to understand process and product risks as a pre-requisite for process validation. • Participate and report to a cross-functional team to advance production activities. • Participate in Operational Excellence activities within Tier Structure. • Participate continuous improvement projects supporting commercial manufacturing site • Ensure systematic DMAIC based approach utilization for process/product related investigations to identify root cause and provide impact assessment to maintain routine manufacturing operations and determine process improvements for manufacturing. • Support technology transfers of launch and commercial cell therapy products • Effectively & efficiently communicate manufacturing process performance internally. • Support the implementation of automation and IT infrastructure projects • Assist in writing technical documentation (protocols & reports for equipment/instrument qualifications, comparability, and cell therapy manufacturing process validation) Skills & Requirements • Bachelors Degree in Biochemical Engineering, Tumor Immunology, Biotechnology or Life Sciences. • Basic understanding in Bioprocessing, Cell Culture and Biochemistry. • Knowledge of ELISA and/or PCR testing • Knowledge in flow cytometry and data analysis (FACSDiva, FlowJo, GraphPad Prism, Excel) is a plus • Ability to think critically, demonstrate troubleshooting and problem-solving skills • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment • Previous experience with other technologies is a plus • Experience with the use of Microsoft word, Excel, Power Point, Smartsheet, Prism, JMP, and other data analysis applications • Highly collaborative with excellent interpersonal, verbal and written communication skills • Ability to think critically with demonstrated problem-solving and troubleshooting skills • Comfortable working in a fast-paced company environment with minimal direction and able to adjust workload/assignments based upon changing priorities • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description

HAYS PLC • Frederick, U.S.

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Research Associate /Senior Research Associate – Translational Biology

A Pharmaceutical Company is seeking an Research Associate /Senior Research Associate – Translational Biology in Lexington, MA. Role Description • Play a role in guiding creative and rigorous biological research programs aimed at fully understanding the disease mechanism of our pipeline. • Conduct efficacy, pharmacokinetic, pharmacodynamics, structure-activity-relationship and mechanisms of action studies of drug candidates • Use appropriate in vivo models to understand the mechanisms by which our drug candidates may contribute to adverse events in patients • Present working progress to team members in group meeting • Work closely with members of our research team to develop in vivo strategies to quickly and effectively address key questions related to the safety and efficacy of our drugs. • Review literature and provide insights to research directions, while predominantly making hands-on contributions to the research Skills & Requirements • Bachelor’s or Master’s Degree in Biology, Pharmacology, or related field, with a minimum of 1-3 years of experience. • Proficient in animal handling, dosing and surgery. Proficient in techniques including but not limited to oral gavage, intravenous injection, subcutaneous injection, blood collection and basic surgery • In depth knowledge of, and hands-on experience with, in vitro and in vivo models used for mechanistic investigation with small molecule or RNAi therapeutics • Experience performing molecular and cellular biology techniques, including but not limited to RNA preparation, RT-qPCR, ELISA, immunohistochemistry, urine biomarker analysis, plasma biomarker analysis • Broad and deep understanding of signaling pathways and biological processes implicated in rare genetic liver diseases as well as the mechanism of action of RNAi therapies is desirable • Previous experience in drug discovery is preferred • Outstanding written and oral communication skills • A high level of motivation and demonstrated record of accomplishment throughout your career • The ability to work effectively as part of a team, in a fast-paced environment

HAYS PLC • Lexington, U.S.

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Sr CRA - Ophthalmology

An American Company is seeking an Sr CRA – Ophthalmology in Rockville, MD. Role Description he Senior Clinical Research Associate (Sr. CRA) will work closely with the Clinical Project manager and is responsible for assisting in the planning and execution of clinical trials which includes assistance in vendor and site management, coordinating or leading data review and cleaning. Will support the CPM with oversight of the clinical study while ensuring the trial is conducted in compliance with the protocol, ICG/GCP, applicable regulatory requirements and applicable SOPs/Work instructions. Candidates must have the ability to prioritize multiple tasks based on workload, work in a fast-paced environment, have strong computer skills (Word Document, Excel and Power Point), maintain completion of required corporate training on standards, policies, work instructions due date. • May act as primary point of contact for specific vendors investigational sites as needed • Create, implement, and maintain systems to track study metrics and general information relating to study execution. Provides the updates to the team on metrics as needed • Prepare trial-related documents including but not limited to Informed Consent Forms (ICF), source documents, patient instruction guides, lab manuals and Case Report Forms (CRFs) • Reviews site-specific study documents (site-specific ICF and study tools/worksheets), , and site payments • Works closely with enablement group and clinical project manager to track study metrics including CRO and other vendor activities • Conduct periodic review of metrics for completion of study files in the eTMF. Escalates appropriately to the CPM and study team of updates and timelines regarding file completion. • Participates in team meetings and may lead small operational teams and/or participates in collaborative efforts (e.g. Standard Operating Procedure (SOP) development, operational task forces, etc.) • Supports Clinical Project Manager in site and vendor selection process, training and evaluation of study personnel (contractors and CRO). • May participate in site visits as needed or accompany experienced clinical monitor for co-monitoring or training purposes • Collaborated with internal cross functional teams to ensure effective delivery of the assigned project milestones • Organizes internal team meetings, investigator, meeting and other trial specific meetings as required • Support the clinical project manager in the planning and organization of investigator meetings and other meetings as necessary • Provides support to the Clinical Project Manager in the management of vendor scope(s) of work, budget updates & reconciliation, as agreed upon with prospectively established milestones and timelines • Maintain completion of required corporate training on standard, policies and work instructions by due date • Generate purchase orders, process vendor invoices and assist in tracking spend approved in the budget • Performs other work-related duties as assigned Skills & Requirements • BS/BA degree in scientific discipline or related healthcare field is preferred but not required; however, the combination of experience and training will be taken under consideration • Minimum 5 years clinical research experience (e.g. pharmaceutical, biotechnology, CRO healthcare setting [including 2 +years monitoring experience is preferred]) • Ability to work on complex or multiple projects and exercise critical thinking • Knowledgeable in clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines, as required • Solid organizational skills, interpersonal skills and communication skills (both written and oral) • Demonstrates problem solving skills, self-motivated and adaptable to a dynamic environment • Strong computer skills (Word Document, Smart Sheet, Excel and Power Point) • Experience in global trials preferred\ • Experience in interactions with vendors (e.g CROs, central laboratories, and other vendors preferred) • Ability to work in a dynamic, fast paced environment • Ability to deal with ambiguity

HAYS PLC • Rockville, U.S.

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