 We are seeking a Regulatory Affairs Specialist to support our national Regulatory Affairs department as well as our Central Regulatory Affairs team in our headquarters in Germany. The Regulatory Affairs Specialist supports the planning and...

The administrator of personal data is &quot;EUROIMMUN POLSKA&quot; sp. z o.o. with headquarters in Wrocław (50-543), ul. Widna 2a (&quot;ADO&quot;). Personal data is processed for the purposes of the recruitment process as well as for the purposes of future recruitment processes, if you give your consent. In connection with the processing of data, you have the right to: access the content of the data and request their rectification, deletion or limitation of processing; data transfer; lodge a complaint with the supervisory authority. More information on the processing of personal data can be obtained at the ADO headquarters or by contacting ADO by e-mail or letter.

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I consent to the processing of my personal data contained in this document by EUROIMMUN in order to conduct the recruitment process. I am aware that I have the right to withdraw my consent to the processing of personal data at any time without affecting the lawfulness of the processing that was carried out on the basis of consent before its withdrawal.

Regulatory Affairs Specialist - In Vitro Diagnostic Medical Devices

Praca Regulatory Affairs Specialist - In Vitro Diagnostic Medical Devices, "EUROIMMUN POLSKA" sp. z o.o.

Regulatory Affairs Specialist - In Vitro Diagnostic Medical Devices

"EUROIMMUN POLSKA" sp. z o.o.O firmie