Global Regulatory Affairs Specialist — EU & Global MAAs

A pharmaceutical company located in Mendrisio, Switzerland is seeking a Regulatory Affairs Specialist to support regulatory compliance and manage submissions for medicinal product registrations. This role requires a Master’s degree in a scientific discipline and 4-5 years of experience in Regulatory Affairs, preferably within the pharmaceutical industry. The successful candidate will work closely with internal teams and external partners to ensure timely and high-quality submissions. A positive work environment and commitment to diversity and gender equality are part of the company culture.
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