Responsibilities

You release raw materials.
You perform QC tests on raw materials and finished products.
You analyse the results and enter them into the system.
You monitor the clean room environment.
You draft product compliance certificates.
You initiate and complete quality events (OOS, deviations, CAPA, etc.).
You participate in reagent management and maintaining the 5S system in the QC laboratory.
You participate in drafting QC test SOPs.
You participate in analytical method validations.
You participate in improvement projects and procedure drafting.

Profil

Bachelor’s degree in a scientific field.
Previous experience in a similar role is an advantage.
Previous experience in the pharmaceutical industry (GMP) is an advantage.
You have strong analytical and summarising skills.
You are precise, rigorous and organised.
You are able to work under pressure and cope with unexpected situations.

Would you like to become a key player in the global fight against cancer?

At Trasis, we offer you the opportunity to work with cutting-edge technologies and contribute to improving cancer diagnosis and treatment techniques. Through your work, you will have the opportunity to make a positive impact on the services provided to users and patients.

The opportunity to participate in building and improving processes in a rapidly growing company.

We offer a young and friendly working atmosphere, a flexible and dynamic environment.

An attractive and flexible salary based on your experience and performance, with extra-legal benefits.

QC Officer