Foccus improvement and development of compliant quality processes.Investigation and follow-up of customer complaints and notifications.Supplier qualification for clean room ISO 8 class (Raw materials).Multi-site processes and QMS documentation alignment.Statistical analysis.Development and control of internal audits: quality process and 5S's.Personnel management.

Documentation Management: creation, translation, training and multi-site alignment.Internal Quality Assurance Audits.Follow up of Pest control activities in site.Issue of certificates of conformity or analysis.Performance and analysis of particle’s control on controlled areas, clean room ISO8 class.Completion of IOPQ activities.

Support to analysts, reagent inventory, documentation, detection of out of specification, quality control on final product, intern statistics.

Study of polymorphism on CbD receptorCell culture management: cell line HeLa, Chang Liver and MCF-7Real time PCR

Medication reconciliation Pharmacological safetyMedical errors detectionHealth campaigns with patients and visitors