Regulatory Affairs Support Intern (all genders)

Opella is a self-care challenger with a strong portfolio in the Over-The-Counter (OTC) and Vitamins, Minerals & Supplements (VMS) market. They are seeking a Regulatory Affairs Support Intern to assist the Regulatory Affairs team in Switzerland with submissions and management of regulatory dossiers. Responsibilities Support for the Regulatory lifecycle management of existing portfolio in Switzerland (medicinal products (Rx and OTC) and medical devices) Contribution to labelling and CMC variations Contribution to Innovation projects (new registration, line extension...) Participation in and coordination of transversal regulatory projects Review of promotional materials Support for the update and review of artworks Organization of administrative documents (PoA, CPP, etc.) Regulatory database maintenance Skills Proficiency in MS Office package and interest in working with database systems Accurate and precise working attitude Strong time management and prioritization skills Team player and good communication skills Project management and organizational skills First experiences in working in a pharma or medical device company would be an advantage University degree in pharmacy or other life science discipline such as Biology, Medicine, Chemistry, etc. is preferred Knowledge in Regulatory Affairs and Swissmedic regulations would be an advantage Fluent in German and English (French or Italian in addition would be an asset) Company Overview Opella is a consumer healthcare business segment of Sanofi. It was founded in undefined, and is headquartered in Neuilly-sur-seine, Ile-de-France, FRA, with a workforce of 10001+ employees. Its website is