Project Manager – Field Corrective Action (Medical Devices)
Location: Zaventem, Belgium | Contract duration: 12 months
Our 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 role
Based 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 responsibilities
- Coordinate and monitor field project activities across multiple countries
- Ensure timely availability and distribution of required maintenance kits and parts
- Follow up on actions performed by internal service teams and external partners
- Ensure activities are completed within defined timelines and quality standards
- Plan and coordinate corrective actions when required
- Consolidate data and provide clear, structured project reporting
- Anticipate needs through forecasting and prioritisation of actions and materials
- Act as a central point of contact for internal stakeholders and partners
- Collaborate closely with the second Project Manager (in Asia) to align priorities on a global level
Your profile
- Proven and successful experience in Project Management is mandatory
- Fluent in English (spoken and written)
- Strong coordination, organisational and administrative follow‑up skills
- Ability to manage multiple priorities in a complex and international environment
- Excellent communication skills and stakeholder management capabilities
- Proactive mindset with strong anticipation, prioritisation and reporting abilities
- Experience in the medical device environment or with field corrective actions is considered a plus, but is not a strict requirement
Practical information
- Project start: mid‑June 2026
- Duration: 12 months
- Working 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 Zaventem
- Flexible office hours aligned with local ( Belgian ) business hours
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