To coordinate QC activities related to outsourcing Technology transfer and/or routine analytical activities .
To ensure that all QC testing related to Tech Transfert are performed according to the established plan, good manufacturing practices, registration product files and site quality standards.
To ensure that the documentation linked to the validation is done according to defined planning to support the establishment of the APR for the commercial and clinical molecule.
To highlight the potential project's issue from a pro-active manner and perform troubleshooting to avoid any project delay...