ICU Medical

Engineer II, AME

ICU Medical

Tijuana, Baja California

Enero 13 2026

Compartir:

Corporativo

Giro

Maquiladora (Export.)

Actividad principal

Manufactura de productos médicos.

Número de empleados

3000

Sitio Web corporativo

Datos de sucursal

Av Calidad No 14409 Internacional Tijuana Tijuana, Baja California

Descripción y detalle de las actividades

Position Summary

Conducts process validation activities related to design transfer and manufacturing improvement projects. Supports strategic initiatives such as CAPAs, remediations, and continuous improvement. Collects BOMs, drawings, and work instructions from Agile for product transfers, including translations.


Essential Duties & Responsibilities

  • Works with the Advanced Manufacturing Engineering team to understand and localize production processes and test requirements.
  • Supports sample builds and the development of local Work Instructions.
  • Supports and/or owns Design Verification and Process Validation build preparation for New Product Introduction (NPI) projects, or as part of CAPA investigations and corrective actions.
  • Validates development tools of moderate complexity and compiles metrics and engineering data, including validation testing outputs.
  • Supports verification and validation protocols issued under NPI projects.
  • Supports and/or leads process validation activities per Master Validation Plans (IQ, Process Characterization, TMVs, CSV, OQ, and PQ), as well as BOM creation, manufacturing procedures, and product unit cost definition.
  • Troubleshoots production line issues, including performing root cause analysis for product, equipment, and system failures.
  • Collaborates with internal departments, vendors, and equipment suppliers to resolve issues and coordinate efforts in support of business objectives.
  • Ensures safety procedures are followed and leads by example.
  • Performs various industrial engineering technical tasks of intermediate scope and complexity, under limited supervision from the direct supervisor or engineering staff.

Experiencia y requisitos

Knowledge & Skills

  • Good analytical, problem solving and project management skills
  • Ability to work in a geographically diverse business environment
  • Ability to leverage and/or engage others to accomplish projects
  • Good verbal and written communications with ability to effectively communicate at multiple levels in the organization
  • Multitasks, prioritizes and respects deadlines. - Good organizational and follow-up skills, as well as attention to detail
  • Site best practices (routings, manufacturing layouts, validations)
  • Process Validations


Minimum Qualifications, Education & Experience 

  • Bachelor’s engineering degree from an accredited college or university is required.
  • +3-5 Years of experience similar role in medical device industry.
  • Demonstrated experience with lean principles


*“Only candidates who meet all the requirements will be considered for an interview.”

Beneficios

  • Beneficios de acuerdo a la LFT
  • Seguro de vida
  • Fondo de ahorro
  • Seguro de gastos médicos
  • Transporte
  • Plan de indexación
  • Utilidades garantizadas
  • Caja de ahorro
  • Servicios medicos en planta
  • Comedor
  • bonos anuales

Número de vacantes 1

Área Ingeniería

Contrato Permanente

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Horario
  • Lunes a Jueves 7:00 a.m. a 5:30 p.m. Viernes 7:00 a.m. a 3:30 p.m.

Estudios Carrera con título profesional

Inglés Hablado: Intermedio, Escrito: Intermedio

Disponibilidad p. viajar Si