Global Pharmaceutical company based near Frankfurt looking for a Regulatory Affairs Consultant for a 6 month period.
An applicant would need to fit the following criteria:
You are responsible for the management of all Regulatory Affairs (RA) activities in Germany to meet current and future RA objectives in alignment with the German Regulatory Affairs objectives.
You formulate short and long term vision for local RA function to ensure functional and internal cross-functions alignment. You act as local RA expert to provide strategic input on the application of local regulations, review processes and submission requirements.
You take ownership for the content of local submission and maintain full awareness of all RA activities on local portfolio, ensuring project deadlines and performance standards are met. You act as the clients representative with local Health Authorities for all regulatory matters.
English and German language is a must.