Quality Specialist Document Control

☞ BioTalent

Ver: 200

Dia de atualização: 26-11-2025

Localização: Zaventem Flemish Brabant Diegem

Categoria: Alta tecnologia Segurança de qualidade / Controle de qualidade Consultoria / Atendimento ao Cliente

Indústria: Medical Devices Consumer Goods Electrical Electronic Manufacturing

Posição: Mid-Senior level

Tipo de empregos: Full-time

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Conteúdo do emprego

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.

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Data limite: 10-01-2026

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