Meet with Zwiers!
Regulatory Affairs (RA) is about science, communication and compliance.
Zwiers Consultancy provides RA/pharmacovigilance service throughout the entire life cycle of medicinal products and medical devices. We are involved in development, market approval and maintenance, ensuring safe and effective use for patients. The RA job is interactive (authorities, experts, team members), scientifically challenging and dynamic, which makes it very rewarding.
Our learn and work program enables young talents to take the step into RA. In the 6 months program they will learn the theoretical essentials, but will also work on an actual assignment. Coached by a Zwiers professional, they get more and more independent and ready to take on a regulatory job. In RA, we look for people with an eagerness to learn, that like teamwork and that have the ability to analyse, interpret and present/write down scientific data.
Interested to learn more about RA, our company and professional opportunities? Meet with us!