{"id":3528124,"url":"https://alion.io/job/philips-clinical-informatics-regulatory-lead","title":"Clinical Informatics Regulatory Lead","company":{"id":13838,"name":"Philips","domain":"philips.com","url":"https://alion.io/company/philips-2","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":85,"open_postings":74,"ghost_share":0,"stale_share":0.797,"repost_share":0,"time_to_fill_p50_days":15,"computed_at":"2026-11-05T05:54:30Z"}},"role":"Biotech","role_family":"Biotech","seniority":"lead","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Best, Netherlands","Bengaluru, India"],"countries":["NL","IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":78187,"max":130312,"currency":"EUR","period":"year","gross":true,"usd_annual":145576},"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"EU MDR","optional":false},{"name":"ISO 13485","optional":false},{"name":"ISO 14971","optional":false},{"name":"IVDR","optional":false}],"status":"live","first_seen_at":"2026-10-30T14:58:40Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-05T10:26:38Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"description":"Job Title\nClinical Informatics Regulatory LeadJob Description\nClinical Informatics Regulatory Lead:\nIn this role you will lead global regulatory strategy for a portfolio of AI-enabled healthcare software, Digital & Computational Pathology, Disease Management Systems, and clinical informatics solutions.\nAs a member of the Clinical Informatics leadership team, you will drive regulatory strategy, market access, lifecycle compliance, and regulatory excellence across global markets while enabling innovation in software, cloud-connected, and AI-powered technologies.\nYour role:\nLead global Regulatory Affairs strategy and execution across the Clinical Informatics portfolio.\nDrive regulatory pathways, submissions, registrations, and market access activities worldwide.\nPartner with R&D, Quality, Clinical, Product Management, Cybersecurity, and Commercial teams on new products, software releases, AI/ML capabilities, and market expansions.\nAdvise senior leaders on regulatory risk, timelines, and business decisions.\nRepresent the company with FDA, notified bodies, competent authorities, and regulators globally.\nBuild and develop a high-performing Regulatory Affairs organization.\nYou're the right fit if you have:\nBachelor's / Master's Degree in Biomedical Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent.\nStrong knowledge of FDA, EU MDR/IVDR, ISO 13485, ISO 14971, MDSAP, and global regulatory frameworks.\n8+ years of Regulatory Affairs experience with significant experience in medical devices and/or IVDs.\nExperience with SaMD, AI/ML-enabled products, cloud-connected solutions, cybersecurity, and interoperability is mandatory.\nProven leadership of global regulatory strategies and complex product portfolios.\nExperience in clinical informatics, digital pathology, radiology, oncology, urology, or diagnostic imaging preferred.\nStrong people leadership, executive presence, and stakeholder influence skills.\nCompensation & benefits for Netherlands\nDoing meaningful work should come with fair, transparent rewards. The base salary range for this role is EUR 78,187.00 - EUR 130,312.00 gross per year. We determine pay within the range using objective factors, like the skills the role requires, your relevant experience and the responsibility you'll have in this role, alongside internal equity and local market considerations.\nThis role is eligible for 3% short term incentive with your rewards linked to both individual performance and company results. We’ll share the full approach with you during the interview process, so you can make a clear, informed decision. Benefits include hybrid working, paid time-off, health and wellbeing benefits, learning and development opportunities.\nHow we work together\nWe believe that we are better together than apart. For this role, this means working in-person at least 3 days per week. \nAbout Philips\nAre you ready to do the work of your life to help the lives of others? Learn more about our business, discover our rich and exciting history and learn more about our purpose.\nIf you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. 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