Beschreibung
Currently I am looking for a Drug Regulatory Affairs Consultant in "Arbeitnehmerüberlassung" to support a global pharmaceutical company in Hessen for a period of 12 months.The role is mainly homebased with a yearly salary of 45.000€-80.000€ depening on the experience.
Major Accountabilities:
- E-CDT Publishing via docuBridge and similar programs
- Life Cycle Management of established products
- Managing marketing authorization submissions (National procedure or/and DCP/MRP)
- Preperation of Variations
- Communicating to local and international authorities
Your Skills:
- 1-5 years of experience in Regulatory Affairs within the pharmaceutical industry
- Strong Communicational skills
- Fluent in English and German
- Good Computer Skills such as Microsoft Office, docuBridge experience is a plus
Next Steps
Please contact Deniz Becker at Real Life Sciences by either contacting me directly on the phone number provided or submitting your CV via the link.
Sthree Germany is acting as an Employment Business in relation to this vacancy.