- Beneficios de acuerdo a la LFT
- seguro de vida
- comedor
- fondo de ahorro
- transporte
- seguro de gastos médicos
- seguro de gastos medicos menores
- Prestaciones Superiores a la LFT
Giro
Medicina
Actividad principal
Manufactura y distribución.
Número de empleados
600
Sitio Web corporativo
Descripción y detalle de las actividades
Ensure achievement of production goals by supervising, coordinating, and optimizing manufacturing lines for medical devices. Guarantee product quality, regulatory compliance, and operational efficiency while developing and guiding the production team in a continuous improvement environment.
- Supervise and coordinate daily production activities to meet output, scrap, productivity, DPPM, and other key performance indicators.
- Ensure compliance with quality standards under medical industry regulations (ISO 13485, FDA 21 CFR 820, GMP).
- Oversee accurate documentation of processes, lot records, and production reports.
- Lead and develop a team of operators, technicians, and line leaders, promoting operational discipline, cross-training, and performance excellence.
- Implement and monitor continuous improvement initiatives (Lean Manufacturing, Kaizen, 5S).
- Collaborate with Engineering, Quality, Maintenance, and Supply Chain to resolve production problems, deviations, and downtime.
- Analyze process, material, and equipment issues, implementing corrective and preventive actions.
- Support product transfers, process validations, and scale-up of new lines or technologies.
- Ensure proper use of equipment, tools, and materials in accordance with Good Manufacturing Practices.
- Enforce safety and hygiene standards within the production area.
- Prepare and present daily, weekly, and monthly performance reports to management.
Experiencia y requisitos
- Bachelor’s degree in Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, Electronics, or related field.
- 5+ years of experience in medical device manufacturing or high‑precision electronics (ideal: hearing aids, implantable devices, diagnostic equipment, sensors, etc.).
- Proven experience supervising production teams of 50+ employees.
- Required experience with ISO 13485 and/or FDA regulations.
- Lean Manufacturing, root cause analysis (8D, Fishbone, 5Why).
- Change control, ECOs, and process validations (IQ/OQ/PQ).
- Ability to interpret technical drawings, specifications, and BOMs.
- Strong understanding of manufacturing KPIs (OEE, FPY, scrap, downtime).
- Experience with ERP/MES systems (SAP, Oracle, etc.).
- Advanced Excel skills (pivot tables, complex formulas, data analysis tools, dashboards).
Beneficios
Número de vacantes 1
Área Producción/Manufactura
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
- Tiempo completo
- Lunes a viernes
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Disponibilidad p. viajar Si

