Project Manager – Field Corrective Action (Medical Devices)Location: Zaventem, Belgium | Contract duration: 12 monthsOur customer is a large, international organisation operating in the medical device sector, with a strong focus on women's health and a significant installed base across multiple regions worldwide.As part of a proactive field project within its Imaging division, our customer is launching a centrally managed corrective action program aimed at ensuring the continued reliability and availability of critical medical equipment used daily by healthcare professionals.The roleBased in Zaventem, you will act as Project Manager / Project Coordinator for an international field corrective action covering Europe and other global regions. You will work closely with a counterpart Project Manager located in Asia, following aligned processes, timelines and reporting standards.Your role is highly coordination‐driven, with a strong focus on planning, follow‐up, communication and reporting.Key responsibilitiesCoordinate and monitor field project activities across multiple countriesEnsure timely availability and distribution of required maintenance kits and partsFollow up on actions performed by internal service teams and external partnersEnsure activities are completed within defined timelines and quality standardsPlan and coordinate corrective actions when requiredConsolidate data and provide clear, structured project reportingAnticipate needs through forecasting and prioritisation of actions and materialsAct as a central point of contact for internal stakeholders and partnersCollaborate closely with the second Project Manager (in Asia) to align priorities on a global levelYour profileProven and successful experience in Project Management is mandatoryFluent in English (spoken and written)Strong coordination, organisational and administrative follow‐up skillsAbility to manage multiple priorities in a complex and international environmentExcellent communication skills and stakeholder management capabilitiesProactive mindset with strong anticipation, prioritisation and reporting abilitiesExperience in the medical device environment or with field corrective actions is considered a plus, but is not a strict requirementPractical informationProject start: mid‐June 2026Duration: 12 monthsWorking model: initially 4 days on site / 1 day remote, with increased flexibility after onboarding (up to 2 or 3 days from home)Office‐based role in ZaventemFlexible office hours aligned with local ( Belgian ) business hours