{"schemaVersion":"jobsearcher.job.v1","id":"344c5b20f32523e1f3ddfd3d","url":"https://jobsearcher.com/jobs/344c5b20f32523e1f3ddfd3d","canonicalUrl":"https://jobsearcher.com/jobs/344c5b20f32523e1f3ddfd3d","title":"Technical Program Manager, Product Development","description":"OverviewIn this role you will lead cross-functional NPD programs for the Light Adjustable Lens (LAL) and accessories from concept to launch. You'll connect R&D, manufacturing, supply chain, quality, clinical, regulatory, and commercial teams to deliver integrated plans, rigorous studies, and compliant documentation. You'll elevate program practices, drive timely delivery, and accelerate time-to-market in a fast-paced, innovative environment. This position offers meaningful impact on patient outcomes and the company's mission to optimize cataract surgery results.ResponsibilitiesLead cross-functional NPD and change control programs from concept through commercial launchDefine integrated NPD program plans with scope, milestones, deliverables, risks and dependenciesLead cross-functional program meetings and ensure decisions and ownership are documented and followed upTranslate user needs and performance targets into structured roadmaps and plansCreate and finalize design history file documentation including risk management, development requirements, and study reportsPlan and lead feasibility, characterization, verification, and validation studies and associated activitiesCollaborate with Regulatory and Quality to align activities with quality systems and submission strategiesCoordinate with Manufacturing Operations and Global Supply Chain for manufacturing transfer and ramp-upProvide clear status updates and dashboards; adjust plans based on new informationImprove program governance, controls, and tailormade processes for scalable executionEnsure smooth handoff from development to manufacturing transfer and production ramp-upFoster proactive cross-functional communication and collaboration across all functionsKey requirementsStrong understanding of regulated medical device product development (requirements definition, feasibility, verification, validation, manufacturing transfer, post-market change control)Knowledge of design controls, quality systems, and risk management (21 CFR 820, ISO 13485, ISO 14971)Excellent analytical and systems thinking for interpreting data and identifying trendsAbility to balance program leadership with hands-on technical contributionExcellent written and oral communication tailored to diverse audiencesProven track record coordinating complex, cross-functional programs to on-time deliveryExperience with project tools (Smartsheet, MS Project) and data systems (Power BI, electronic quality management system)Experience with external partners (consultants, test labs, suppliers)Self-motivated, proactive, and able to work with minimal supervisionBachelor's degree in Chemical Engineering (or closely related) + 6+ years in medical device development; 3+ years leading cross-functional teamsExperience with GMP/GDP/GLP a plusstrong communicationcross-functional collaborationproactive problem-solvingSmartsheetMS ProjectPower BI","company":"Rxsight","rawCompany":"rxsight","city":"Irvine","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-10-26T13:44:09.494Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339115","title":"Ophthalmic Goods Manufacturing","slug":"ophthalmic-goods-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Technical Program Manager, Product Development","description":"OverviewIn this role you will lead cross-functional NPD programs for the Light Adjustable Lens (LAL) and accessories from concept to launch. You'll connect R&D, manufacturing, supply chain, quality, clinical, regulatory, and commercial teams to deliver integrated plans, rigorous studies, and compliant documentation. You'll elevate program practices, drive timely delivery, and accelerate time-to-market in a fast-paced, innovative environment. This position offers meaningful impact on patient outcomes and the company's mission to optimize cataract surgery results.ResponsibilitiesLead cross-functional NPD and change control programs from concept through commercial launchDefine integrated NPD program plans with scope, milestones, deliverables, risks and dependenciesLead cross-functional program meetings and ensure decisions and ownership are documented and followed upTranslate user needs and performance targets into structured roadmaps and plansCreate and finalize design history file documentation including risk management, development requirements, and study reportsPlan and lead feasibility, characterization, verification, and validation studies and associated activitiesCollaborate with Regulatory and Quality to align activities with quality systems and submission strategiesCoordinate with Manufacturing Operations and Global Supply Chain for manufacturing transfer and ramp-upProvide clear status updates and dashboards; adjust plans based on new informationImprove program governance, controls, and tailormade processes for scalable executionEnsure smooth handoff from development to manufacturing transfer and production ramp-upFoster proactive cross-functional communication and collaboration across all functionsKey requirementsStrong understanding of regulated medical device product development (requirements definition, feasibility, verification, validation, manufacturing transfer, post-market change control)Knowledge of design controls, quality systems, and risk management (21 CFR 820, ISO 13485, ISO 14971)Excellent analytical and systems thinking for interpreting data and identifying trendsAbility to balance program leadership with hands-on technical contributionExcellent written and oral communication tailored to diverse audiencesProven track record coordinating complex, cross-functional programs to on-time deliveryExperience with project tools (Smartsheet, MS Project) and data systems (Power BI, electronic quality management system)Experience with external partners (consultants, test labs, suppliers)Self-motivated, proactive, and able to work with minimal supervisionBachelor's degree in Chemical Engineering (or closely related) + 6+ years in medical device development; 3+ years leading cross-functional teamsExperience with GMP/GDP/GLP a plusstrong communicationcross-functional collaborationproactive problem-solvingSmartsheetMS ProjectPower BI","datePosted":"2026-10-26T13:44:09.494Z","dateModified":"2026-10-26T13:44:09.494Z","hiringOrganization":{"@type":"Organization","name":"Rxsight","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Irvine","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"344c5b20f32523e1f3ddfd3d"},"url":"https://jobsearcher.com/jobs/344c5b20f32523e1f3ddfd3d"}}