1. QbD
2. Belgium, The Netherlands
3. Clinical, Qualification & Validation, Quality management, Regulatory affairs, Software validation
Are you an expert within medical devices and passionate by helping companies in this area in their growth or to achieve their ISO13485 certificate? Apply now for the job of medical devices specialist at QbD!
Table of Contents
As a QbD medical devices engineer you will be working on several projects within ISO13485 environments or you will help companies achieve their ISO13485 certificate. You are a communicative versatile person, capable of solving problems, investigating root causes and implementing changes.
What do we expect from you as a Medical Device Specialist?
4. You are capable of conducting internal audits regarding ISO13485, Quality management systems, Quality Assurance, …
5. You will be responsible for the implementation/maintenance of Quality Management Systems according to ISO13485
6. You have an eagle eye for optimizations within quality and quality systems and are able to implement them
7. In this role you work in close collaboration with production, QA, engineering, QC, process/validation engineers, supply chain, …
8. We count on you for the development of a Standard operating Procedure (SOP), related Work Instructions (WI), forms, checklists, protocols, reports
9. As a project consultant you are responsible for the tracking and reporting on project deliverables
10. You are able to coach a small team but also to work independently
11. You are responsible for preparing all documentation for filing to authorities
12. We expect you to follow regulations on medical devices and share your insights/knowledge within the QbD team and at our customers
13. You support in setting up the timelines for the go-to market strategy in light of the applicable regulations and the customer’s business plan
Who are we looking for?
14. Scientific master’s degree : engineer (bio, industrial, civil), industrial pharmacist, …
15. Experience in the life science industry and in GMP, preferably in medical device projects
16. Knowledge on quality system standards (ISO 13485), regulatory standards for Medical Devices (21CFR820 & EU MDD/MDR) or software used for Medical Devices (IEC 62304) is a big plus
17. First experience with audits is an advantage
18. Good project management skills
19. A true QbD’er can be recognised by the following qualities: Resilient: Your strong and positive attitude helps you overcome any challenge Hungry for knowledge : You are always open to learning No BS mentality : you can be straightforward in a respectful way Innovative : You are constantly looking for new and better solutions (Not too) serious : your job is serious, but you don’t take yourself too serious.
What does QbD Group offer you?
An attractive and complete salary package:
20. A monthly wage, car, fuel card, (super fast) bicycle, insurance package, meal vouchers, etc.
But most of all…
21. We offer sustainable careers and meaningful connections
22. We are a knowledge based company
23. You’ll work for an award winning company: Best Managed Company (Deloitte award), Baanbrekende Werkgever, …
Our promise to you:
24. As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
25. Moreover, we aim to create a joyful community where you dare to be and can be yourself. Because the best way to grow is by growing together as unique individuals.
26. In short … We stand for JPEG : J oy in P artnership, going for the E xtra mile to G et things done!
Interested?
Send us your CV and motivation letter and who knows, maybe you’ll find your #QbDream job.