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Regulatory Affairs Associate

The company
Our client is an innovative global pharmaceutical company with a single goal to contribute to improving healthcare, such as the development of new vaccines and ensuring that everyone has access to affordable, high-quality medicines.

Role Description 
As a Regulatory Affairs Associate  you will ensure that the products have legal permission to be released on the market for sale. You will act as an intermediary between our client’s project teams and the regulatory bodies. It is essential that you are on top of Dutch law and legislation. Your job also includes maintaining efficient communication channels.

Responsibilities 
-Supports, prepares, and completes moderately complex regulatory submissions, which require interactions with cross-functional groups

-Helps review regulatory content and packages for completeness and accuracy
-Ensures own work complies with established practices, policies and processes, and any regulatory or other requirements.
-Ensuring regulatory compliance in the packaging and according to the law - legislation policies to ensure completion of the end-to-end process
-Ensure our client’s internal databases are updated in a timely manner

Requirements
-Minimum 3 years of relevant working experience

-BSc or MSc Degree, preferably in Pharmaceutical or Biochemistry field
-Experience in Regulatory Affairs in Local Market
-Excellent communication skills in Dutch and English

Other information
Our client is seeking to highly motivated talents for different positions, do you want to join them and be part of an exciting journey in the development of innovative vaccines. If you are interested or know someone who is, contact me via the apply button. I would be happy to discuss this opportunity with you.