Juan Jose Fierro Email & Phone Number

Argentina

Responsable por los mercados de Bolivia y Paraguay.

Argentina

Argentina

Audit ManagementQuality Management systemCold Chain QualificationQuality Operations, Quality oversight of the manufacturing activities as well as collaborating closely on the process with the Head of Batch Release. • Managing the Quality oversight over the LSP operations (“on the floor”).• Approving investigations following deviations and related CAPAs.• Executing In Process Testing and Sampling activities (per instructions and procedures approved by SENASA).• Act as the main point of contact with the Corporate Product Quality Manager for Change Control (product related), Annual Product Reviews, and Process Validation program.

• Responsible for conducting In process quality checks and approval of Line clearance for dispensing, Manufacturing and packaging activities. • Review of batch manufacturing records• Works strongly to ensure and maintain a high level of quality system audit readiness.• Redaction and approval Standard Precedures.• Actively participates in internal audits or external audits.• Reviews and dispositions the following Documents: change controls, SOP, protocols, reports. • Assures that cGMP and safety training for all QA personnel is conducted in a timely, efficient and complete manner in order to meet regulatory compliance requirements.• Assures manufacturing processes are in compliance with corporate standards as well as regulations including; cGMP• Implement KPI´s.• Assures timely action and closeout of commitments made by the different groups (Change Control Action request, investigations, audit, inspection audits).

• Development and Implement KPI´s • Development manufacturing processes in compliance with corporate standards as well as regulations including; cGMP – SENASA.• Ensures adequate capacity balance between testing, QA and release teams. • Identifies capital projects that would results on cost reduction/avoidance.• Identifies technology improvement opportunities and implements site strategies for acquisition of equipment.• Supports the implementation of network wide systems• Assures the appropriate interaction of support groups such as QA, QC, Technology, Engineering & Maintenance, Materials Management, Regulatory Affairs, Safety and Labor Relations group.• Cold Chain Proyect.• Development Traceability Proyect.

• Responsible for Regulatory Affairs Argentina • Compliance manager.• Compilation of Annual Product Review Report• Actively participates in internal audits or external audits.• Reviews and dispositions the following Documents : change controls, SOP, protocols, reports. • Assures that cGMP and safety training for all QA personnel is conducted in a timely, efficient and complete manner in order to meet regulatory compliance requirements.

Medico Clinico Privado.

Medico Veterinario, Veterinary Medicine

Posgrado - Especialista En Calidad Industrial, Quality Management

Auditor Dgq, Inti

Auditor Ambiental, Auditor

Modelo de gestión de la Norma ISO14000, con un esquema educativo de Aspects International (Reino Unido) reconocido por EARA (Environmental.

Evaluacion De Laboratorios De Calibración Y Ensayo, Inti