After an exclusive partnership with a fully integrated specialty vaccine company, I am looking for experienced Regulatory Affairs professionals to join them in a senior position.
The company are committed to developing and commercializing innovative vaccines against infectious diseases, including Typhoid, Cholera and Hepatitis A.
As a Regulatory Affairs manager you will be responsible for the compilation, publishing, submission and archiving of all variations, and the implementation of Regulatory Affairs processes including eCTD submissions.
The preparation of Regulatory documentation for submissions are another key part of this role, which involves preparing clinical trial applications, marketing authorization applications, variations and renewals. Another key duty is to authorize and draft all texts, as well as review documents from other departments.
- Master's degree in life science discipline
- 5 years Regulatory Affairs experience
- Project management experience
- Fluent in German and English
If you feel you have what it takes, get in contact now!