PstrongALTEN Italy /strong, a leading force in the IT, Engineering and Life Sciences industries, is on the lookout for a vibrant and driven strongSystem Engineer /strong to join our team in the Life Sciences industry. /ppWithin 30 years, strongALTEN /strong has become a leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics Space, Defense Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors. /ppstrongWhat are we looking for? /strong /ppWe are looking for a System Engineer that supports our Hardware Team in development activities related to analyzers and related ancillary devices for In-Vitro-Diagnostic (IVD) applications. /ppstrongResponsibilities: /strong /pulliParticipate to define, update and review requirements. /liliReview the associated hardware specifications. /liliInteract with the other development areas within System Development Integration Department (“Software”, “Consumables” and “Assay Integration”), as per the joint development/improvement tasks. /liliInteract with external Partners, as per the joint development/improvement tasks. /liliChallenge the technical solutions proposed by development partners. /liliManage hardware installations aimed at hardware testing activities. /liliEdit, review and perform hardware verification/validation plans. /liliContribute actively to troubleshooting with the instrument development Partners. /liliInvestigate on anomalous and/or uncommon situations. /liliInteract with other Company functions, in order to provide System Development Integration know-how and support to problem solving. /liliEnsure compliance with the Code of Ethics, the Quality Management System, the Company Policies and the Corporate Procedures. /li /ulpstrongRequirements: /strong /pulliMaster’s Degree in Mechanical Engineering, Mechatronic Engineering or equivalent. /lili≥ 5 years experience, particularly in development activities regarding mechanics/automations. /liliPrevious experience in IVD (In Vitro Diagnostics) and/or highly regulated FDA environments is appreciated. /liliKnowledge of GMP (Good Manufacturing Practice) is appreciated. /liliSeasoned experience using Microsoft Office package. /liliKnowledge of CAD SW will be a plus. /liliFluent spoken and written Italian and English. /li /ulh3Seniority level /h3ulliAssociate /li /ulh3Employment type /h3ulliFull-time /li /ulh3Job function /h3ulliConsulting /li /ulh3Industries /h3ulliIT Services and IT Consulting, Engineering Services, and Medical Equipment Manufacturing /li /ul #J-18808-Ljbffr