Beschreibung
More Details:* 12 Months fulltime
* Location: Berlin or Zug
* Start date: a.s.a.p.
Areas of responsibility:
* You can write submissions by yourself (for EU, Asia, and Africa).
* You have post-approval regulatory CMC experience.
* You can author and review post approval CMC variations intended for submission to Health Authorities globally.
Recruitments:
* You are high experienced in writing global CMC-Submissions (min.10 years).
* You are fluent in English and be able to write dossiers in English.
* German or fresh is a plus
For a confidential discussion about regulatory affairs projects in Switzerland, or to apply, then send your CV to or call me.
I am a specialist recruitment consultant in regulatory affairs for the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on Switzerland.
If you are a Pharmaceutical professional looking for your next opportunity, then please don't hesitate to get in contact with me. Alternatively if you are currently looking for skilled individuals for the development of your organisation, then I can certainly help.
Your personal contact:
Kristina Bröckel
Regulatory Affairs Consultant
Tel:
mailto:
To find out more about Real please visit www.realstaffing.com