Description
Manager Regulatory Affairs (m/f)
Reference: -en
Start: 06/18
Duration: 6 MM
Main tasks:
- 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 Merck representative with local Health Authorities for all regulatory matters
Main qualifications
- Advanced degree in Pharmacy/Chemistry/Biology or other science-related field
- Profound experience in pharmaceutical regulatory affairs is required
- Working knowledge of key health authorities in Germany and surrounding European countries
- English (business fluent)
Main advantages:
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.