• Issuance and update of master documentation; specifications and analytical methods for raw material and finished product, packaging material and their arts, Standard Operating Procedures and work instructions.• Generation of master data; product and material codes, barcodes, package labels, expiration dates, materials lists and inspection plans through SAP.• Management, distribution and approval of electronic documents through the MasterWeb system.• Participation in new projects; generation of documentation for the launch of new products.• Attention, follow-up and compliance to Minister of Health audits and requirements (COFEPRIS-Mexico, INVIMA-Colombia, ANVISA-Brazil, ANMAT-Argentina and DIGEMID-Peru).• KPIs follow-up and implementation of strategies for their improvement.• Application and implementation of CAPA plans and change controls.• Follow-up on any result out of specification, deviations or quality risks in inputs and products.• Participation in internal and external audits.• Safeguarding, distribution and control of documents.

• Issuance and update of master documentation; specifications and analytical methods for raw material and finished product, packaging material and their arts, Standard Operating Procedures and work instructions. • Review that the documents entering the documental system meet the requirements of good manufacturing and documental practices. • Management, distribution and approval of electronic documents through the ENAXIS system. • Application and implementation of CAPA plans and change controls. • Follow-up of non-conformities, results out of specification, deviations and complaints.• Management of databases (finished product, raw materials and packaging materials). • Safeguarding, distribution and control of documents.

• Issuance and update of the documentation generated in the department. • Verify the closing of manufacturing and conditioning orders, physical-chemical and microbiological results of the finished product for product release.• Application of Corrective and Preventive Actions plans and change controls derived from manufacturing processes.• Follow-up to change controls, non-conformities, assembly of dossier and Annual Product Review.• Safeguarding, distribution and control of documents.

• Release of areas and equipment for manufacturing.• Verification and sampling of raw material and finished product.• Approval of bulk product and execution of process controls from the manufacturing stage to conditioning.• Detect and record nonconformities and results out of specification.• Management of ANSI sampling tables and statistical tools.

• Preparation of antimicrobial and oncological mixtures and parenteral nutrition, guaranteeing their correct dosage and their sterile grade.• Conditioning and identification by SAP system of the mixtures.

Worked in the research project "Detection of the accumulation of fatty acids in the mitochondria of the liver of Wistar rats with metabolic syndrome", using experimental methods of gas chromatography, liquid chromatography (HPLC), spectrofluorometry and western blot.