Your responsibilities :

Define, develop and validate analytical methods and other control methods implemented (internal & external);
Develop the transfer of new analytical methods as well as the optimization of existing methods;
Develop a QC/analytical knowledge network;
Propose and implement new technologies of quality control thanks to the identification of opportunities of innovation within the projects thanks to a technological and bibliographical watch;
Ensure the follow-up and control of subcontracted laboratories (specifications, audits, costs,…);
Define and justify sampling / controls and specifications (final QC/IPC);
Carry out unannounced quality control operations;

Your profile :

Master/PhD scientific orientation (Chemistry, biochemistry…)
Good knowledge in analytical (assay/purity), HPLC, GC, MS, NMR, IR, titration
Knowledge of ISO/GMP standards
Theoretical and practical knowledge of GMP standards
Experience in validation, analytical transfer and stability
Excellent knowledge of French
Good knowledge of English (B1-B2)
Autonomy
Synthesis and analysis skills
Mastery of the office suite

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.

Analytical Chemistry Specialist