You are responsible for the data collection and transmission into to the cGMP database PRIMR. Moreover, you administer documentations from external stakeholders. You need to provide in a timely manner, an exact and reliable entry of the process data into the systems and other related analytic tools.
Administrator Data Collection 50% Pharmaceutical Industry
- KV / Büro
Within the Pharmaceutical Industry globally & successfully operating company.
A dynamic working environment where multi-cultural teams from all over the world are working together. You will find generous working conditions.
High-School diploma, or similar
1-2 years of experience in a similar position, pharma/biotech industry and GMP knowledge are beneficial. You are strongly motivated to work and organize you on your own and take initiative to get the job done. Moreover, you are a good communicator, written as well as oral, especially in English. You are used to work with MS-Office tools, as Excel, Word and PowerPoint on a daily base. If you are the one we are looking for, please apply to Nadin Schwarzenbach, email@example.com. We look forward to reading from you.
Englisch: Very good
This position is offered for one-year with a 50% work quota and with a strong option to get extended. Client reference number BIOBJP00002396 (please integrate in your application).