Requirements: English
Company: JR Italy
Region: Varese , Lombardy
Social network you want to login/join with:Medical DeviceOrganizational Area: MolecularCountry / State: ItalyHome / Office based: Office basedReporting To: Global SD&I System Integration ManagerYOUR MISSIONThe Global Systems Integration Engineer is responsible for executing activities throughout the product development lifecycle, including:Feasibility testing and optimizationDevelopment activities, including system verification and validationAssay integration and validationAssessing and supporting system reliabilityProblem solving related to software, hardware, consumables, and assay integrationHands-on troubleshootingRequirements management and product definitionYOUR CONTRIBUTIONSWork on the development and integration of systems and subsystems designed for medical diagnostics, including instruments, related equipment and fixtures, software, consumables, and assay protocols and chemistries.Write system requirements/specifications.Review hardware and software requirements/specifications.Perform system feasibility, optimization, and verification & validation activities in line with other key functions in the company. Write and execute test protocols for system-level testing.Assess system reliability and support reliability testing activities.Present work and experimental results to key stakeholders through high-quality PowerPoint presentations.Ensure the quality of technical documentation in compliance with all the company''s requirements, including Quality Assurance requests.Work cross-functionally with other company functions (including R&D, Quality Assurance, Corporate Service, Business, and Operations) to drive successful product development and own technical expertise on systems integration competencies.Collaborate with third-party instrumentation suppliers on instrument development, as required by the project.EducationMasters Degree in Engineering or Sciences, preferably with emphasis on Biomedical Engineering.ExperienceMinimum of 3 years in a systems engineering, systems integration, or product development role.Demonstrated technical proficiency, scientific creativity, collaboration, and a successful track record involving independent thinking.Preferably, experience working in the medical device industry, developing products subject to CE marking or FDA approval.SkillsHighly motivated and success-driven.Understanding of system-level product development.Ability to understand interfaces between components in a complex product.Ability to present complex problems through high-quality PPT presentations and effectively lead to proper decision-making.Scientific background in the molecular field is an advantage.Ability to escalate issues appropriately.Strong analytical problem-solving and decision-making skills.Good organizational and interpersonal skills.LanguagesEnglish: Fluent or native language, both written and spoken.Italian: Fluent or native language, both written and spoken.#J-18808-Ljbffr