Several Regulatory Affairs (RA) Contracts: Labelling, CMC, International Submissions, Publishing-Switzerland 6 to12 months
If you are looking for your next project in a well-established Biotech company that is truly dedicated to grow and develop into a Biotech leader worldwide, then look no further and read below.
Due to my client's expansion they are looking for several Regulatory Affairs professionals to help with the extra workload or new projects across several areas as: CMC, Labelling, International submissions and Emerging Markets or Publishing.
In order to be successful within this role you will need experience in Regulatory Affairs in either Pharma or Biotech with specialised expertise in one or more of the following fields: CMC, Labelling, International Submissions or Publishing. Fluency in German is a nice to have but not a must.
The length for each project can differ from 6 to 12 months, and in general there is a high possibility of extension to be expected as my client is continuously starting new projects. In some cases, remote working is either partially or fully applicable which will give you the flexible to gain a good work life balance.
Experience in within the EU is needed. Please note we can only accept applications from candidates who hold valid European Union passport and are able to work in Europe without visa sponsorship.
For a confidential discussion send your CV to email@example.com, Elena Cazacu, Senior Recruitment Consultant for Switzerland.