Quality Assurance Specialist
il y a 18 heures
We are seeking a highly skilled Quality Assurance & Regulatory Affairs Manager to join our team at Covartim 2021. As a key member of our Quality Assurance & Regulatory Affairs team, you will play a crucial role in ensuring the compliance of our clients' medical devices with regulatory frameworks.
Key Responsibilities:- Implement Quality Management Systems at our clients, based on our developed systems.
- Develop regulatory strategies for the introduction of innovative medical devices on the market.
- Perform projects for our clients in our office in Brussels and Liège.
- Good understanding of Medical Devices and IVD regulatory environment (directives, regulations).
- Good knowledge of Medical Devices quality assurance (ISO 13485, 21 CFR) and relevant standards.
- Speak French/Dutch and English to communicate with our clients and team.
- Make clients' satisfaction a priority by combining quality and professionalism.
- A comfortable, spacious, and colorful office surrounded by greenery.
- Meal vouchers (8 euros/day), supplemental health insurance (DKV Belgium), and complementary pension.
- Public transport costs fully covered and compensation for the usage of your own car.
- One well-being workshop per quarter (yoga class, nordic walk, seated massage, cooking class,...).
We are looking for a motivated and experienced professional to join our team. If you are passionate about medical technologies and have a strong background in quality assurance and regulatory affairs, we encourage you to apply.
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