http://www.AdriaCanada.com

Manage Integrated Systems (Quality, Safety & Health, Environment). Suppliers audits, complaints, risk assessments (FMEA).• Lead transfer to manufacture.• Provide support to the development area of ​​the region.• Analysis of CAPAs, OOS, Complaints, and suppliers' nonconformities• Approval of SOPs, checklist, WI, and any other document types.• Implementation of ISO 9001 and Regional Company harmonization.• Planning of Bench Trials, stability tests, and… Show more Manage Integrated Systems (Quality, Safety & Health, Environment). Suppliers audits, complaints, risk assessments (FMEA).• Lead transfer to manufacture.• Provide support to the development area of ​​the region.• Analysis of CAPAs, OOS, Complaints, and suppliers' nonconformities• Approval of SOPs, checklist, WI, and any other document types.• Implementation of ISO 9001 and Regional Company harmonization.• Planning of Bench Trials, stability tests, and validation of new sources and new manufacturing sites. • Savings (packaging, and raw materials).• Tollers´ and suppliers´ audits.• Data analysis and metrics for QMR, KPIs, and other reportable forums.Key achievements • Dozens of TTM with Zero defect• Developed of new tollers• Reduction in single sources • Saving and benchmarking for the region with logistic and packaging improvements• Circular economy (boxes)• Customer centricity Show less

Quality Assurance, Quality Control, and Regulatory Affairs. Also, environmental and sustainability projects. • Lean Project Management.• Responsible for QA and QC.• Develop Staff training program according to the gaps.• Lead client visits and audits, as well as members of the management. Attend inspections and audits.• Prepare performance reports for the Direction of the Company. • Coordination of inter laboratories and analysts´ qualification.• Compliance with… Show more Quality Assurance, Quality Control, and Regulatory Affairs. Also, environmental and sustainability projects. • Lean Project Management.• Responsible for QA and QC.• Develop Staff training program according to the gaps.• Lead client visits and audits, as well as members of the management. Attend inspections and audits.• Prepare performance reports for the Direction of the Company. • Coordination of inter laboratories and analysts´ qualification.• Compliance with Environmental requirements. • RSE, and Environmental aspects.Key achievements • Substantial improvement in the results of third-party audits, which implied maintaining the most important accounts of the company and the expansion of the portfolio. All that was thanks to the leadership and commitment of the staff, including the high direction.• GMP implementation• 19 Key Elements re certification• ISO 45000 implemented• Training of new internal auditors• Highly improvement on supplier performance• Implementation of the Program Zero Pellet loss® Operation Clean Sweep® (OCS).• Reduction of special waste 80% the first year and 30% the second yearTrainer in:• Metrology, calibrations, validations, and statistical control of processes. Show less

• In Charge of Quality Assurance, Quality Control (microbiological, physics, and chemical aspects), and Regulatory Affairs.• Audits and inspections from customers and authorities (FDA, SENASA, ISO, IFS, BRC, A&B, Kosher, Halal).• GMP-FSA, HACCP, and IFS trainer.• Batch records and tracking • Management of change responsible• FMEA owner • Risk assessment report and action plans• Lead regulatory submissions and inspection readiness activities• Pray for the… Show more • In Charge of Quality Assurance, Quality Control (microbiological, physics, and chemical aspects), and Regulatory Affairs.• Audits and inspections from customers and authorities (FDA, SENASA, ISO, IFS, BRC, A&B, Kosher, Halal).• GMP-FSA, HACCP, and IFS trainer.• Batch records and tracking • Management of change responsible• FMEA owner • Risk assessment report and action plans• Lead regulatory submissions and inspection readiness activities• Pray for the fulfillment of the company policy, GMP, regulatory domestic and LATAM affairsKey achievements • ISO 9001 Recertification• IFS Implementation• SAP implementation• Relocation of the laboratory Show less

• Quality Management System (ISO/TS 16949 ISO 9001) and Quality Control. Follow-up (maintenance) and recertification.• Attend customer complaints• Coordinate actions for OOS, CAPAs, and any manufacturing issue• Adequate SOPs and floor informationKey achievements Key achievements • Recertification of IATF16949.• Preparation and leading daily staff meetings• Significant improvement in customer satisfaction survey

• Auditor in ISO 9001, ISO 14001.• OSHAS and IFP.• Consultant in ISO 9001, ISO 14001, IRAM, GMP, HACCP and API.

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• Development of the Certification Area, technically and commercially. (ISO, EU, NM, • ASTM, API, IRAM) • Environmental mediator.Key achievements• Create from scratch material characterization laboratory and obtain the accreditation of ISO 17025 accreditation.• Certification of ISO 65 and ISO 9001. • Consultant of the Health Minister on the regulation of phthalates in toys and babies'items NM583/2008. Regulated in… Show more • Development of the Certification Area, technically and commercially. (ISO, EU, NM, • ASTM, API, IRAM) • Environmental mediator.Key achievements• Create from scratch material characterization laboratory and obtain the accreditation of ISO 17025 accreditation.• Certification of ISO 65 and ISO 9001. • Consultant of the Health Minister on the regulation of phthalates in toys and babies'items NM583/2008. Regulated in 2011.https://archive.org/stream/Boletin_Oficial_Republica_Argentina_1ra_seccion_2011-04-11/2011-04-11_djvu.txt Show less

• Oversee the analysts who perform stability tests, analyse the results, and write reports.• Bench trials -replacement of chemicals on the red list and savings- • Responsible for MSDS, and packaging approvals for dangerous goods.• Represented the Quality department on the ISO 9001 committee. (Certification process was ongoing)• Audit the pilot batch and first productions of new formulations.• Salesforce trainer in GMP