Celerion Switzerland AG is part of the global Celerion Inc. With our European GLP-certified bioanalytical facility located in Fehraltorf / Zürich, as a contract research organization (CRO) we are supporting the pharmaceutical and biotechnology industries during the development of new drugs and products.
To support our bioanalytical laboratory we are looking for a
Technical Writer (m/f) (100%)
You will be the responsible person to write study reports for bioanalytical and method validation studies performed in our GLP testing facility. You will prepare draft reports on the basis of recorded study data, and work in close collaboration with the responsible study directors to issue final study reports within the contracted timelines.
Assignment start: as soon as possible
Contract duration: 12 months (option for prolongation or change into unlimited contract will be checked at the given time)
Do you have questions? Contact our HR Manager Iris Rüttimann by email or phone 043 355 76 76.
How to get into contact? Please send your complete application by email or mail to:
Information for recruiting agencies: For this position Celerion is not willing to take any unasked applications by recruiting offices. Thanks for your understanding.