Description
Global Regulatory Affairs Manager (m/f)
Reference: -en
Start: 09/18
Duration: 4 MM
Main tasks:
- Manage the regulatory submission process through to approval including management and coordination of the preparation of all regulatory documentations in cooperation with external partner(s), as applicable
- Support the Marketed Product Leader in executing regulatory strategies and project managing regulatory submissions in partnership with GRA’s external strategic partner while working closely with the Global Regulatory Marketed Products Operations Management group
- Contribute to development and evaluation of regulatory strategies for projects (under supervision of the Marketed Product Leader)
- Member of the Regulatory Subteam
- Close cooperation with headquarter and country regulatory affairs functions worldwide
Main qualifications
- Degree in a Life Science or related discipline, higher degree preferable (PhD, MSc, MBA)
- Interest into Scientific details
- Knowledge of international regulatory affairs
- Prior exposure to Regulatory Affairs preferably in a global position
- Several years of industry experience with at least 8 years’ regulatory experience
Main advantages:
- A very renowned company
- Access to a Germany-wide network of 3,000 companies
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.
My contact at Hays:
My contact person:
Esat Yaktubay
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