{"id":1512976,"url":"https://alion.io/job/livanova-senior-system-verification-engineer","title":"Senior System Verification Engineer","company":{"id":1949485,"name":"LivaNova","domain":"livanova.com","url":"https://alion.io/company/livanova","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":75,"open_postings":8,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-06T05:45:30Z"}},"role":"DevOps","role_family":"DevOps","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Italy"],"countries":["IT"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":43000,"max_usd":89000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":15},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":true,"technologies":[{"name":"Jira","optional":false},{"name":"MATLAB","optional":false},{"name":"Python","optional":false}],"status":"live","first_seen_at":"2026-09-16T00:00:00Z","employer_posted_date":"2026-09-16","last_verified_at":"2026-10-06T22:02:48Z","board_verified":true,"closed_at":null,"days_open":20,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":20},"description":"As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow-because at LivaNova, we don’t just treat conditions - we aspire to alter the course of lives.\nWho are we looking for:\nAre you passionate about testing complex systems and ensuring that innovative medical devices meet the highest standards of safety, performance, and regulatory compliance?\nWe are looking for a Senior System Verification Engineer to join our R&D team and play a key role in the verification of integrated hardware and software medical devices throughout the product development lifecycle.\nIn this role, you will lead system-level verification activities, working closely with Systems Engineering, Software, Hardware, and Quality teams to ensure product requirements are fully verified and documented according to international standards and regulatory expectations.\nYour new role:\nLead the definition and execution of system verification strategies for complex medical devices.\nTranslate system requirements into comprehensive verification plans, protocols, test cases, and traceability matrices.\nExecute and coordinate system-level testing activities, including functional, performance, usability, and safety verification.\nCollaborate with Systems Engineering, Software, Hardware, and Quality teams to ensure complete requirements coverage.\nAnalyze test results using statistical methods and prepare technical reports to support product development decisions.\nInvestigate verification failures, identify root causes, and support corrective actions.\nManage verification activities, including planning, scheduling, resource allocation, and progress tracking.\nEnsure verification documentation is audit-ready and compliant with applicable regulatory requirements.\nSupport risk management activities and contribute to product safety assessments.\nContribute to regulatory submissions and support internal and external audits.\nMentor junior engineers and promote best practices in system verification and validation.\nDrive continuous improvement initiatives related to verification processes, methodologies, and tools.\nHow you'll make an impact:\nEnsure that medical devices are thoroughly verified and meet customer, quality, and regulatory requirements.\nContribute to the development of safe, reliable, and high-performing healthcare technologies.\nSupport successful product launches through robust verification planning and execution.\nStrengthen collaboration between engineering disciplines and quality functions.\nImprove product quality by identifying issues early in the development lifecycle.\nEnhance verification effectiveness through process improvements and technical leadership.\nHelp maintain compliance with global medical device standards and regulations.\nAbout you:\nBachelor's or Master's degree in Biomedical Engineering, Electronic Engineering, Systems Engineering, or a related technical field.\n3+ years of experience in Verification & Validation (V&V), System Verification, or Testing within the Medical Device industry or other highly regulated sectors.\nProven experience verifying complex systems involving both hardware and software components.\nStrong understanding of requirements management and traceability principles.\nKnowledge of medical device standards and regulations, including:IEC 60601\nISO 13485\nISO 14971\nFDA regulations\nEuropean MDR\n\nExperience with requirements and defect management tools such as DOORS, Jira, or similar platforms.\nFamiliarity with statistical analysis tools such as Minitab, Excel, or equivalent tools.\nBasic programming or scripting experience with Python, MATLAB, or similar languages.\nUnderstanding of embedded systems, hardware-software integration, and software validation principles.\nStrong analytical and problem-solving capabilities.\nExcellent communication and technical documentation skills.\nAbility to work effectively within multidisciplinary and cross-functional teams.\nFluent English, both written and spoken.\nWhat you will find:\nThe opportunity to contribute to the development of innovative medical technologies that improve patients' lives.\nExposure to the full medical device product development lifecycle.\nA highly collaborative environment involving Systems, Software, Hardware, Quality, and Regulatory teams.\nThe chance to work on technologically advanced products within a regulated industry.\nOpportunities to expand your expertise in Verification & Validation, Risk Management, and Regulatory Compliance.\nTechnical leadership and mentoring responsibilities with visibility across multiple functions.\nContinuous learning and professional growth within a dynamic international organization.\nLocation: Mirandola, Italy\nWHAT WE CAN OFFER YOU:\nNational Collective Bargaining Agreement: CCNL Gomma Plastica\nLevel: A/C\nBase Salary range: € 31.000 - € 50.000\nBonus: 0-5%\nActual compensation will be determined based on relevant experience, qualifications, and internal equity considerations.\nWe offer a competitive benefits package including:\nFlexible working options.\nMedical insurance.\nPension scheme.\nEmployee stock purchase plan.\nGlobal recognition programme.\nAdditional benefits (e.g. meal vouchers, flexible benefits, local bonuses) may apply depending on location.\nIn addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with a competitive package, including financial and wellbeing benefits.\nIf you like the sound of the above and feel energised by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!\nWelcome to impact. Welcome to innovation. 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