A global pharmaceutical company is seeking a Regulatory Affairs Lead in Baar, Switzerland. This role requires a professional to manage local regulatory affairs, ensuring compliance with Swissmedic and FOPH/BAG. Responsibilities include preparing marketing authorization applications, maintaining regulatory data, and facilitating market access. The ideal candidate will have at least 5 years of regulatory affairs experience in the pharmaceutical sector, particularly with Swiss regulations, along with a strong educational background in pharmacy or life sciences.
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