Beschreibung
- Zurich
- 3 Months contract guaranteed with extension possible
- Replacement of longterm sickleave
- Immediate start needed
- Possibility to work 80%
Regulatory Affairs Manager (m/f/d)
Reference: -en
Start: asap
Duration: 3 MM+
Main tasks:
- Regulatory tasks concerning the entire life cycle of a drug
- Regulatory document review
- Health authority interaction (Swissmedic)
- CMC (ICH) variation checks
- Submission of documents to health authorities
- Cover letter writing (no regulatory writing)
Main qualifications
- M.SC. Master of Science
- Perfect knowledge C2 level of German and English
- Eye for details
- Qualitative working method
- Preferable first industry experience
- Preferably some reading knowledge of French AND/OR Italian
Main advantages:
- Being part of a Global Pharma company
- Possibility to learn a lot
- Being part of a great team of 12
- Cross functional work in Regulatory
- Flexible way of working with possibility to work partly remote in disussion with your manager
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:
Jadie Ann Vallons
Referencenumber:
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