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Our client is an international healthcare company focused on medical devices and wellness products that contribute to everyday consumer well-being.
The European organization operates in multiple countries, combining strong local presence with international expertise. It is known for multiple, well-known brands.
The culture is dynamic, transparent, and entrepreneurial, emphasizing collaboration, responsibility, and innovation.
Quality Assurance - Temporary - Medical Devices (Hybrid)
Functieomschrijving
As a Temporary Quality Assurance Coordinator - Medical Devices, you will ensure the quality of medical devices, working closely with internal teams and external suppliers to guarantee compliance with regulations and quality standards.
This temporary role offers the opportunity to gain experience in a regulated, international environment, with a hybrid work model and a strong focus on collaboration and quality management.
Key responsibilities
- Drive quality: Own supplier relationships and manage all quality agreements.
- Ensure compliance: Lead change control and product quality processes, ensuring all modifications follow protocol and regulatory standards.
- Support QMS activities, documentation, and operational QA processes.
- Collaborate with colleagues and report critical activities to your line manager.
Profiel
- Max. 5 years of working experience in regulated industries (pharmaceutical is a plus)
- ISO13485/MDR knowledge is a plus.
- Fluent in English; Other languages are an asset.
- Social, proactive and solution-oriented.
Aanbod
- Temporary role in a international environment (+/- 6 months)
- Hybrid working model: 2-3 days at the Ghent office, remaining days remote
- Flexible schedule: 3/5, 4/5, or full-time
- Competitive compensation package