Dieses Inserat auf JobHeidi
For our customer in the pharmaceutical industry we are looking for a - Regulatory Affairs Manager (m/ w) MOC004-199 - Your responsibilities:
- Compilation, updating and submission of registration dossiers, variations and re-submissions
- Editing of amendments and leaflets
- Responding to requests from authorities, providing answers on deficiency letters in time and with high quality
- Preparation and review of drug informations
- Ensuring good interaction with authorities
- Collaboration with internal and external departments
- Provide development teams with regulatory input and strategies
Your responsibilities: - University degree in science (pharmacy, chemistry, biochemistry)
- 2 – 5 years of experience in Regulatory Affairs
- Experience in compiling eCTD dossiers is desired
- Good organizational skills
- Good knowledge of MS Office applications
- Fluent in English and very good command of German and/or French (written & spoken)
- Strong communication skills, hands-on attitude and the ability to work independently as well as in a team
- Are you interested? Then please send your complete documents (if possible as PDF-file) to
Waltraud.bueb@nemensis.com - Nemensis ag, the human factor. Your competent recruitment partner specialized in chemistry, biology/biotechnology, pharmaceutics, medical device/engineering and health care. - Frau Dr. Waltraud Bueb freut sich auf Ihre Kontaktaufnahme oder die Zustellung Ihrer kompletten Bewerbungs- unterlagen an: - nemensis ag - Kägenstrasse 18 - Postfach 557 - CH - 4153 Reinach (BL) - Tel: +41 61 205 98 98 - Fax: +41 61 205 98 99 -
www.nemensis.com -
job@nemensis.com
