The organisation of sample management plays a central role within the customer. Analysis samples are taken during the manufacture of pharmaceutical and chemical products at various stages of production. The analysis samples must be recorded, distributed to the internal and external QC laboratories, stored and disposed of at the end of their shelf life. There are numerous interfaces to the research and QC laboratories, warehouses, production, planning and external contract laboratories. The daily interaction with local and global, internal and external partners makes the job varied and exciting. Good communication, solution-oriented and systematic work, as well as organisational talent are the key to success in this multi-faceted, responsible role.

WHAT WILL YOU DO?

Organisation and implementation of sample collection and sample distribution of commercial finished pharmaceutical products, raw materials and active ingredients, packaging materials and medical devices.
Coordination and realisation of sample shipments to external test laboratories, as well as transfer and control of analysis results from external test laboratories in eLIMS.
Carrying out and documenting temperature analyses of sample and product shipments.
Carrying out visual comparative tests of primary packaged sterile products during the release of internally manufactured products or as part of the incoming inspection of externally manufactured bulk goods.
Creation and maintenance of SOPs and work instructions in the area of responsibility.
Collaboration in the creation and processing of non-conformances and change requests in Trackwise, as well as assistance in the definition of corrective and preventive actions (CAPA).
Collaboration in local and global projects.

WHO ARE YOU?

Professional experience in a GMP-regulated environment, preferably in the field of quality control, is an advantage
Very good organisational and communication skills, customer-oriented way of working and "can do" mentality
Very good knowledge in the use of Microsoft Office programmes
Experience in the control of analysis data and GMP documents, as well as experience in working with SAP, eLIMS and Trackwise are an advantage
Very good knowledge of German and English (written and spoken)

WHAT DO WE OFFER?

Exciting and varied tasks in the environment of the life science industry
Development opportunities in an internationally growing company
A dynamic team that attaches great importance to a collegial and open atmosphere
Attractive employment conditions with an excellent occupational pension fund
1st class accident insurance (private)
Additional benefits such as daily meal allowances
Academy days and team building events
International onboarding
Flexible working hours, 5 weeks holiday
Homeoffice - the possibility of working from home

READY TO APPLY?

Have we caught your attention and would you like to become #partofAgidens?

Then we look forward to receiving your complete application documents with CV, copies of diplomas and references.

If you have any questions, please contact Mrs Esther Iacuzzo, HR Professional, on +41 (0)61 713 00 80. In writing via email to: esther.iacuzzo@agidens.com

We look forward to hearing from you!

QC Specialist