Mission OverviewWe are seeking an experienced Temporary Project Manager to lead, on a day-to-day basis, the definition, execution, and monitoring of a comprehensive regulatory compliance action plan for EU Class II and Class III medical device technical documentation.Operating in a high-pressure and time-critical environment, the Project Manager will play a pivotal role in ensuring full alignment with applicable international medical device regulations, while coordinating and mobilizing all relevant internal and external stakeholders.Key ResponsibilitiesDrive the daily planning, coordination, and execution of the medical device technical documentation compliance action plan.Ensure timely progress, clear prioritization, and rigorous follow-up against defined objectives and regulatory deadlines.Act as the central point of coordination across multidisciplinary teams (Regulatory Affairs, R&D, Quality, Clinical, Manufacturing, External Partners, etc.).Establish strong cross-functional collaboration and foster a culture of accountability and results.Anticipate risks, manage escalations, and implement corrective actions as required.Provide clear, structured, and transparent reporting on progress, issues, and mitigation plans to local management and Group Top Management.Ensure alignment with applicable European and international regulatory frameworks for medical devices.Operating ContextThis role is set within a demanding environment characterized by regulatory urgency and the need for intense cross-departmental cooperation. Success requires strong leadership, decisiveness, and the ability to align diverse stakeholders toward unambiguous objectives and fixed timelines.The Project Manager will have full legitimacy, authority, and active support from both local management and Group Top Management to successfully deliver the mission.Candidate ProfileThe successful candidate will demonstrate the following mandatory qualifications and attributes :Proven and formal training in project management methodologies (mandatory).Demonstrated experience and solid knowledge of medical devices and relevant international regulations (EU MDR and related frameworks).Fluency in Italian is required; proficiency in English is necessary for communication with the holding group.Strong leadership and facilitation skills, with the ability to federate teams around common objectives.Natural authority, credibility, and the capacity to drive decisions in complex and pressured environments.Excellent communication, organizational, and stakeholder management skills.Why Join This MissionThis assignment offers a high-impact opportunity to play a critical role in a strategic regulatory compliance initiative, with strong executive sponsorship and decision-making authority, in a context where results, leadership, and execution excellence are paramount.This job posting is open to candidates of all genders, in compliance with applicable laws (L. 903 / 77 and L. 125 / 91).#J-18808-Ljbffr