OncoBeta® GmbH is specialized in the development and commercialization of innovative therapies with radioisotopes. Currently, we offer a novel brachytherapy for the individualized treatment of non-melanoma skin cancers.
An important team member supporting the further regulatory affair and quality management evolution of OncoBeta GmbH, a medical device organization, as well as its sister business units or subsidiary companies. OncoBeta is a quick growing company in size and regulatory/ quality management scope. Critical needs exist in oversight of the quality management system, audit preparation and work related to the migration from MDD to MDR, the medical device quality framework governing CE.
What to Expect:
Expect to work in a dynamic, transparent, open, friendly, hardnosed and international team. We are always aiming to do our best. Expect to push yourself and to grow as an individual. Expect to be treated fairly, with dignity and to be given significant responsibility and freedom to manage big initiatives.
Training will be provided where needed to ensure continued expertise in the below quality management frameworks.
This is an opportunity to participate in a rapid global expansion involving many different Regulatory Affairs entities and Quality Management guidelines.
Sound like the right job for you?
If you would like to become a part of the OncoBeta® team, please send us your CV including recommendation letters with your earliest entry date as well as your salary expectations.
by e-mail to firstname.lastname@example.org
by mail to OncoBeta GmbH – Attn. HR – Quality Management – Lichtenbergstraße 8 – 85748 Garching n. Munich – Tel.: +49 (89) 5484224 0