QA Documentation Specialist

  • Location: braine l'alleud
  • Type: Contracting
  • Job #18627

QA Documentation Specialist

Brabant Wallon – contracting 

#QA #Deviation #CC #CAPA

Our partner is looking for a QA Documentation Specialist to join its team. This international company is well-known for its pharmaceuticals and vaccines. 

What are your responsibilities?

You will be responsible to support the migration of data, records and documents from one system to another in compliance with the data integrity and our partner’s processes. Here are your main tasks:

  • Support creating an inventory of the documents and records
  • Control, generate and ensure correct metadata with the support of impacted stakeholders for each document according the requirements of the target system and the original record
  • Support all activities related to the migration of documents in compliance with the Good Documentation Practice, data integrity requirements and our partner’s processes (migration documents, maintain traceability matrix, review and support on the validation protocol, etc)

Who are you?

  • You hold a Scientific bachelor’s degree
  • You have 3 years of experience in pharmaceutical regulated environment
  • You have good knowledge of Deviation, Change control, CAPA implementation
  • You are a team player and autonomous
  • You have some good ICT tools (MS office, Sharepoint, Trackwise, Veeva,…)
  • You speak English and French

What can you expect?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. 

You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact Sophie Rolis: [email protected] or +32497/51.50.92

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