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 https://www.opella.com.
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