Management Systems Specialist
13485:2016, FDA (21 CFR Part 820) and NOM-241-SSA1-2021 requirements). CAPA/Deviation administration. Monitoring trends...
13485:2016, FDA (21 CFR Part 820) and NOM-241-SSA1-2021 requirements). CAPA/Deviation administration. Monitoring trends...
/studies. Prepare and follow up on site and country audits, CAPA preparation and implementation. Accountable for resource...
quality policy in all activities. Manages the NCR and CAPA process by documenting, investigating, root cause analysis... and Preventive Action (CAPA), Critical Thinking, Customer Centricity, Feasibility Studies, Lean Supply Chain Management...
compliance to the quality policy in all activities. Manages the NCR and CAPA process by documenting, investigating, root cause...
. Manage deviations, investigations, CAPA, change control, complaints, non-conforming products, recalls, and quality risks... storage and distribution practices, risk management, deviations, investigations, CAPA, change control, audits, inspections...
(CAPA), Complaints, Self-Inspections /Audits, Risks systems, among others Quality systems. Works closely with Quality...
de causa raíz, planes de acción y cierre de acciones de las desviaciones encontradas. Ante cualquier documento CAPA al área...
to setup MES for new products. · To follow up the execution of DA、ECN and CAPA (Corrective Action and Preventive Action...
materials to authorized third-party laboratories for analysis. Manage non-conformances, LIRs, and CAPA action plans...
de causa raíz, planes de acción y cierre de acciones de las desviaciones encontradas. Ante cualquier documento CAPA al área...