Regulatory Affairs Associate

il y a 5 jours


Zaventem, Belgique Abbott Laboratories Temps plein

Abbott is recruiting a Regulatory Affairs Associate to be based in our office in Zaventem.

The Regulatory Affairs Associate supports the Sr. EMEA Regulatory Affairs Specialist with implementation of regulatory activities in the Benelux region.

**Role and Responsibilities**:

- Support new product introductions and tender activities by providing appropriate regulatory and quality documentation as required in the region.
- Gather, evaluate, and organize RA documentation in different formats and provide submission documentations to ensure they contain all necessary details and adhere to applicable regulatory standards.
- Review, analyze and approve advertising & promotional materials
- Ensure compliance with regulation requirements for advertising & promotional materials.
- Performs other related duties and responsibilities, as assigned.
- Support the Sr. Regulatory Affairs Specialist EMEA as required, to meet local business objectives.
- Perform administration duties when required.
- Able to work efficiently in an office environment as well as remotely when needed.

**Your Profile**:

- Educated to a degree level, graduate in a scientific area preferably
- Must be proficient in English, Dutch and French
- Competent user of Microsoft Office packages. Strong working knowledge of Excel and SharePoint is desirable.
- Strong attention to detail.
- Time management and problem-solving skills.
- Critical thinking and inquisitive; able to carefully assess the importance, relevance and validity of the information gathered.
- Must be a team player, with the ability to work independently. Flexibility and the ability to cope with varying workload and demands as required are needed.


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