Hovione is an international company with over 55 years’ experience in the development and compliant manufacture of Active Pharmaceutical Ingredients and Drug Product Intermediates.
With four FDA inspected sites in Portugal, the U.S., Ireland and China, Hovione offers integrated API, particle design, formulation development and GMP manufacturing.
In the inhalation area, Hovione is the only independent company offering such a broad range of services.
To reinforce our team we are looking to fill the following position at our Lumiar site :
The Procedures and Qualification Specialist will be respnjsible for identify and perform documentation work related to new or updated practices to implement on B14 analytical activity.
Will also be responsible to define and support Laboratory s installation and equipment requirements. Plan and support equipment acquisitions, transference and installation.
Facility logistics management and documentation update. Be able to support B14 analytical area after the implementation.
Main responsibilities :
We offer :