Quality Control Officer

at  Trasis

As a Quality Control Officer you will carry out operations and controls to validate the conformity of Trasis products.

Your responsibilities:

• Perform quality checks (raw material/In-process/finished products and stability) and record results.
• Approve or reject raw and packaging materials.
• Ensure the availability of certificates of conformity when receiving consumables.
• Write certificates of conformity for products;
• Participate in improvement projects and procedure writing;
• Approve labels after first printing
• Manage the sampling of consumables.
• Plan and organize quality control subcontracting operations (raw materials / process / finished products and stability).
• Receive and encode the results of the subcontracted laboratories and file the documents.
• Evaluate that the results of the controls are in conformity with the specifications.
• Verify batch records (MBR,…).
• Write certificates of analysis and conformity.
• Manage stability samples.
• Manage clean room monitoring and ensure out of specification monitoring and reporting.
• Communicate deviations and malfunctions and propose improvements

Your profile :

• Bachelor degree in a scientific field.
• A first experience in a similar position is an asset.
• A first experience in the pharmaceutical field (GMP) is an asset.
• You have an analytical and synthetic mind.
• You are precise, rigorous and organized.
• You are stress resistant and able to deal with the unexpected.

We offer :
Do you want to become a major player in the global fight against cancer?
At Trasis, we give you the opportunity to work with cutting-edge technologies and to contribute to the improvement of cancer diagnosis and therapy techniques. Through your actions, you will have the opportunity to have a positive impact on the services provided to users and patients.
The opportunity to participate in building and improving processes in a growing company.
We offer a young and friendly work atmosphere, a flexible and dynamic environment.
An attractive and flexible salary according to your experience and performance, with extra-legal benefits

• Perform quality checks (raw material/In-process/finished products and stability) and record results.
• Approve or reject raw and packaging materials.
• Ensure the availability of certificates of conformity when receiving consumables.
• Write certificates of conformity for products;
• Participate in improvement projects and procedure writing;
• Approve labels after first printing
• Manage the sampling of consumables.
• Plan and organize quality control subcontracting operations (raw materials / process / finished products and stability).
• Receive and encode the results of the subcontracted laboratories and file the documents.
• Evaluate that the results of the controls are in conformity with the specifications.
• Verify batch records (MBR,…).
• Write certificates of analysis and conformity.
• Manage stability samples.
• Manage clean room monitoring and ensure out of specification monitoring and reporting.
• Communicate deviations and malfunctions and propose improvement