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B. Braun is a major international company and a leading provider of the global health care market.
The Global Regulatory Affairs department and Pharmaceutical Product Lifecycle Management is an important part of the organizational structure of B. Braun.
Internally it lies at the interface of drug development, manufacturing, marketing, pharmacovigilance and clinical research. Externally it is the key interface between the company and the regulatory authorities.
In our Global Regulatory Affairs Pharmaceutical department, we are developing regulatory strategies and managing regulatory procedures/ marketing authorizations successfully.
The scope of duties includes all necessary activities to apply for new registrations in new countries and maintain up to date the registration dossier of already approved products.
Your main tasks:
Become part of a corporate culture that actively promotes constructive exchanges between colleagues, customers and partners. We can offer you interesting, varied tasks and excellent opportunities for advancement, as well as an attractive salary and benefits, all within a dynamic family-owned company.