descrizione del lavoro

pstrongGlobal Systems Integration - Molecular Medicine /strong /ppstrongOrganizational Area: /strongMolecular /ppstrongCountry / State: /strongItaly /ppstrongPlace of work: /strongBresso (MI) /ppstrongHome / Office based: /strongOffice based /ppstrongReporting To: /strongGlobal SDI System Integration Manager /ppbr/ppstrongJob Scope /strong /ppThe Global Systems Integration Engineer is responsible for executing activities through out the product development lifecycle including: /pulliFeasibility testing and optimization /liliDevelopment activities, including system verification and validation /liliAssay integration and validation /liliAssessing and supporting system reliability /liliProblem solving related to software, hardware, consumables, and assay integration /liliHands-on troubleshooting /liliRequirements management and product definition /liliRisk management /li /ulpbr/ppbr/ppstrongMain Responsibilities /strong /ppbr/pulliWork on the development and integration of systems and subsystems designed for medical diagnostics, including: instruments, related equipment and fixtures, software, consumables, and assay protocol and chemistries. /liliWrite System requirements/specifications /liliReview hardware and software requirements/specifications /liliPerform system feasibility, optimization, and VV activities in line with other key functions in the Company. /liliWrite and execute test protocols for system level testing /liliAssess system reliability, and support reliability testing activities /liliPresent workand experimental result, to key stakeholders, through high quality PowerPoint presentations /liliEnsure the quality of technical documentation in compliance with all the Company's requirements including Quality Assurance requests /liliWork cross-functionally with other company functions (including RD, Quality Assurance, Corporate Service, Business, and Operations) in driving successful product development and owning technical expertise on systems integration competencies /liliWork with 3rd party instrumentation suppliers on instrument development, as required by the project. /li /ulpbr/ppstrongEducation: /strong /ppMaster’s Degree in Biotechnology. /ppstrongSpecialization/PhD: /strongMolecular Medicine (Appreciated but not required) /ppbr/ppstrongExperience: /strong /ppMinimum of 3 years in a systems integration, or product development role /ppbr/ppstrongTechnical Competencies: /strong /ppbr/ppDemonstrative technical proficiency, scientific creativity, collaboration and a successful track record that has involved independent thinking. /ppPreferably the candidate should have experience working in medical device industry, developing products that are subject to CE marking or FDA approval. /ppbr/ppstrongSkills: /strong /ppHighly motivated and success driven /ppUnderstanding of system level product development /ppAbility to understand interfaces between components in a complex product /ppAbility to present complex problems through highest quality PPT presentations and effectively lead to proper decision making /ppScientific background in molecular field is an advantage /ppAbility to escalate issues appropriately /ppStrong analytical problem solving and decision making skills Good organizational and interpersonal skills /ppGood communication skills /ppbr/ppstrongLanguages: /strong /ppEnglish: fluent or mother language, both written and spoken /ppItalian: fluent or mother language, both written andspoken /p