Quality Specialist Document Control
Vue: 200
Jour de mise à jour: 26-11-2025
Localisation: Zaventem Flemish Brabant Diegem
Catégorie: Haute technologie Assurance Qualité / Contrôle Qualité Conseil / Service client
Industrie: Medical Devices Consumer Goods Electrical Electronic Manufacturing
Niveau: Mid-Senior level
Type d’emploi: Full-time
le contenu du travail
This is a well-established medical device company based in Zaventem, Belgium. They have been able to become a leader in the industry with their gold standard, groundbreaking technology at the core. They are expanding rapidly, even doubling their growth in the past 4-5 years. This opportunity offers a lot of flexibility and the chance for an outgoing quality professional to travel to other countries, whilst working within a collaborative and passionate work environment.
Key Roles & Responsibilities
- Facilitate & improve the process management of the PLM
- Responsible for the interface between departments to ensure the appropriate changes are properly documented.
- Work with change order originators to ensure change orders and other related change documents are written in accordance with procedure.
- Organise EQMS change development, implementation & approval
- Follows standard practices and procedures when analysing situations or data. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
- Makes sure that existing procedures and standards are followed
- Responsible for providing agile-related trainings & support for users
- Ensure all applicable requirements are applied and maintained
- Maintenance of quality documents, including archiving
Skills & Requirements
- 2+ years’ experience in a Document Control/Engineering Services/Quality/Regulatory role preferred
- ERP experience (desired but not essential)
- Fluent in written English
- Exposure to various cultures
- Experience maintaining & improving the QMS
- ISO13485 experience (desired but not essential)
If you want to be part of an innovative, growing company where you can expand your current knowledge, GET IN TOUCH - Please email me your CV at louise.cleland@biotalent.com and we can arrange confidential chat.
Date limite: 10-01-2026
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