The role of a Qualified Person is pivotal in ensuring batches intended for clinical trials meet EU GMP and Product Specification File requirements.
Duties:
* Responsibilities include reviewing and certifying batches to adhere to regulatory standards.
* Maintenance of site licenses through inspections by health authorities.
* PARTICIPATION IN ONGOING COMPLIANCE ACTIVITIES related to clinical trials, including technical agreements with collaborators.
This is an excellent opportunity for a skilled professional to join a leading multinational organization.