Execute and document new product development projects, input suppliers development, engineering changes and commercial products service, meeting technical and documentary requirements for manufacturing, packaging, quality control and enabling, throughout the entire product life cycle.

In charge of bioterium administration (only QC bioassays, not intended for non-clinical testing), team building, applicable regulations, operation starting, regulatory permissions, reliability of analytical reports and analytical methods validation/verification, animal health and wellbeing assurance, team and resources management

In charge of special projects, project management of plant based product development, negotiation, strategy, team building, strategic planning, market research

Technical assistance to commercial products, new presentations, national and international regulation, biosimilar products development, feasibility, formulation, analytical methods, pilot batches production, stability studies, thecnical documentation, pharmaceutical technology, transference process

Executed online patent research regarding formulations, active substances, manufacturing processes and treatment methods of new pharmaceutical products specially biopharmaceutical or biotechnological products, emiting patent landscape reports