PpCosmo is an innovative company focused on medical technologies (MedTech), active in the development of solutions based on artificial intelligence, dermatology, gastrointestinal diseases, and CDMO services. We collaborate with global partners to improve the quality of care and patients’ lives. Our mission is to build trust in health through scientific and technological innovation. /p h3Key Responsibilities /h3 h31. Program Planning Execution /h3 ul liDevelop detailed project plans, schedules, and work breakdown structures covering all phases of customer programs. /li liCoordinate engineering, AI, systems, clinical, quality, and regulatory workstreams to ensure alignment with program objectives. /li liDefine clear milestones, dependencies, and deliverables for internal teams and external partners. /li liMonitor progress and drive accountability for on-time, high-quality execution. /li liMaintain accurate program documentation and ensure consistent communication of status. /li /ul h32. Customer Program Coordination /h3 ul liServe as the day-to-day program management interface for customer teams. /li liFacilitate regular customer touchpoints, progress reviews, and issue-resolution discussions. /li liTranslate customer requirements into structured inputs for engineering and CQRA teams. /li liEnsure alignment on scope, timelines, deliverables, and change-management processes. /li /ul h33. Risk, Issue, and Change Management /h3 ul liIdentify and track program risks, issues, and blockers across engineering, regulatory, and operational domains. /li liDrive mitigation strategies and cross-functional problem solving. /li liManage scope changes through structured review and impact assessment with internal teams and customers. /li liEnsure escalation paths are clear and followed when critical risks emerge. /li /ul h34. Cross-Functional Leadership /h3 ul liPartner with Product Engineering, CQRA, and Commercial to ensure programs are delivered efficiently and compliantly. /li liAlign cross-functional teams on priorities, staffing needs, and resource allocation. /li liSupport preparation for design reviews, quality gates, regulatory milestones, and customer audits. /li liPromote structured decision-making and documentation discipline across teams. /li /ul h35. Regulatory Quality Coordination /h3 ul liEnsure project activities follow applicable processes, including design control, risk management, verification, validation, and quality documentation. /li liCoordinate CQRA input into program plans, regulatory timelines, and submission-relevant deliverables. /li liSupport readiness for regulatory milestones and submission activities owned by the company or customer teams. /li /ul h36. Operational Excellence /h3 ul liContribute to the continuous improvement of program management frameworks, templates, and best practices. /li liSupport capacity planning and forecasting across programs. /li liEnsure lessons learned are captured and integrated into future programs. /li /ul h3Qualifications /h3 h3Required /h3 ul liBachelor’s degree in Engineering, Life Sciences, Computer Science, or related field. /li li5+ years of experience in project or program management within medical devices, digital health, or other regulated technology domains. /li liStrong understanding of structured product development processes, including design control and risk management. /li liExperience coordinating cross-functional teams spanning engineering, quality, regulatory, and operations. /li liExcellent communication, organization, and stakeholder-management skills. /li liAbility to manage multiple programs concurrently in a dynamic and evolving environment. /li /ul h3Preferred /h3 ul liExperience managing programs involving Software as a Medical Device (SaMD), AI-enabled technologies, or medical electrical equipment. /li liFamiliarity with EU MDR, FDA pathways, and quality system expectations (ISO 13485). /li liExperience working in customer-facing or contract-engineering environments. /li liPMP or equivalent project management certification. /li /ul pOccasional travel up to 20 to 30 percent for customer meetings, audits, workshops, and cross-site team collaboration. /p h3Equal Opportunity Statement: /h3 pWe support equal opportunities, without any discrimination; The research complies with Legislative Decree 198/2006 /p /p #J-18808-Ljbffr