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    Regulatory Affairs Specialist

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About the company:
Our client is a well-known global company with a specialization in healthcare. They are guided by a strong dedication to improve people’s live through science

About the role:
In this role, you will be working for a project in which all labelling documentation have to be submitted. Moreover, you have to ensure proper compliance regarding the industrial implementation steps

- This role requires data management ability which consists the following; Veeva database updates: creation of database, uploading documents, date entry submission and approval. Vista: launch of artwork and quality check
- Beside the data management, you will also contribute to the quality check of artwork, labeling texts and provide support in continuous variations

- Three years’ experience in Regulatory Affairs
- Good understanding of Regulatory Affairs legislation