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 expanding new and existing approvals as well as notices of nonconformity in Switzerland and the EU
Coordinating processes with the 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 field (EU, Switzerland), preferably with herbal medicines.
Knowledge of Regulatory Information Management (RIMS) software and electronic databases such as SPOR and 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 client specializes in the development, production, and distribution of herbal medicines (phytopharmaceuticals), foods, and dietary supplements made from fresh plants. Distribution takes place both nationally and internationally through pharmacies, drugstores, as well as health food stores and supermarkets. The approximately 170 employees in Switzerland embrace independence and personal responsibility every day in a family-like environment. Work location: Rohrschach
