What will you learn?

- To develop and manufacture medicines and pharmaceutical products on an industrial scale at agreement in accordance with the legislation in force and the advances in science and technology.

- To be responsible for the industrial organisation, monitoring and control of drug manufacturing processes and to coordinate the whole of Departments involved in manufacturing.

- Ensure the implementation of Good Manufacturing Practice for Medicines.

- Assess that each batch of medicinal products is manufactured, controlled and stored in accordance with the law and the terms of the marketing authorisation.

- Coordinate and manage the release of each batch of medicinal products, certified for conformity and quality by appropriate documents and records.

- To know the appropriate design of industrial plants and to promote their update and renovation, as well as the modernisation and maintenance of premises and equipment.

- Apply quality by design in the manufacture of medicines in relation to Public Health and promote the rational use of medicines.

- Learn how to prepare and approve the technical documentation generated during the development of a medicinal product that allows its approval by the health authorities.