You are responsible for the entire life cycle process of the herbal medicinal products
Create and update chemical-pharmaceutical regulatory dossiers (with focus on CMC /Module 1) and production information.
Updating and extending new and existing approvals, as well as deficiency letters in Switzerland and the EU
Coordinate processes with marketing, medical and development departments.
Development of strategies for new products and their market launch
Close cooperation with national and international partners
Your profile
Completed scientific studies (pharmacy, biology, chemistry) or comparable qualification
Several years of professional experience in a relevant regulatory affairs area (EU, CH), preferably with herbal medicinal products.
Knowledge of Regulatory Information Management Software (RIMS) and in electronic databases such as SPOR, Eudravigilance/Art 57 is a plus.
Very good oral and written English and German skills
Good knowledge in resp. great interest in the field of phytopharmaceuticals
Extremely accurate and structured way of working
Your advantages
Varied and international cooperation
Familiar working atmosphere and appreciative corporate culture
You can take on responsibility and develop both professionally and personally.
Our customer
Our customer specializes in the development, production and distribution of herbal medicinal products (phytopharmaceuticals), foodstuffs and food supplements made from fresh plants. The products are distributed nationally and internationally via pharmacies, drugstores, health food stores and supermarkets. The 170 or so employees in Switzerland live their independence and personal responsibility every day in a family environment. Place of work: St. Gallen region
