Amphenol CMT - Critical Medical Technologies

Ingeniero de Calidad II

Amphenol CMT - Critical Medical Technologies

Tijuana, Baja California

Hace 21 horas

Compartir:

Giro

Manufacturera

Actividad principal

Ensamble de productos médicos.

Número de empleados

400

Datos de sucursal

Av. Ferrocarril 17030 16y1 Niños Héroes (parque Industrial Los Pinos) Tijuana, Baja California

Descripción y detalle de las actividades

Is responsible for ensuring the safety and quality of our products and procedures through rigorous inspections, implementation of quality control measures, and identification of areas for improvement, collaborates with cross-functional teams to address quality issues, drive continuous improvement, and contribute to building high-quality products that exceed customer expectations. Quality Engineer possess a strong background in engineering or quality assurance, attention to detail, and a proactive mindset.

• This position can develop and manage Quality Control Technicians.

• Contribute to all cost saving and safety initiatives and related CIS programs.

• Generate and maintain process requirements, specifications, validation and confirming quality documents to assure product / component conformance.

• Develop and execute test method validations.

• Develop and maintain FMEA’s and Control Plans.

• Perform, maintain, and sustain activities under QMS.

• Ensure that FI, CAPA, NMCRs and Customer complaints are addressing in a timely manner.

• Coordinate and/or contribute in DHRs processes.

• Document a quality alerts and coordinate investigations for NCMR, CAPA, FI and Customer Complaints.

• Generate a weekly and monthly reports using quality objectives.

• Provides support during audits and /or customer visits.

• Participate in the performance of the environmental management system in accordance with current roles and responsibilities.

Experiencia y requisitos

  • Bachelor’s degree in engineering (industrial, chemical, manufacturing, or any other related).
  • And/or 3 years on QA/QC engineering work experience on QA/QC in medical device manufacturing processes such device assembly, injection molding or extrusion, preferable.
  • Preferable ISO 13485 certified internal auditor.
  • Knowledge by school or work experience in risk Management analysis, FMEA – Control Plans management, statistical data analysis on Minitab, preferable, Test Method validation and GR&R execution, root cause analysis technics management, CAPA – Complaint - NCMR execution and management.
  • Experience in Lean and Kaizen participation and execution is preferred.
  • Negotiation and leadership skills.
  • Advanced Computer skills (Minitab, Office, Word, Excel, Power Point, and/or Application Programs, Statistical Software, Databases. Etc.).

Beneficios

  • Beneficios de acuerdo a la LFT
  • Comedor subsidiado
  • Fondo de ahorro

Número de vacantes 1

Área Calidad

Contrato Permanente

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Horario
  • Lunes a viernes
  • Turno Matutino

Estudios Carrera con título profesional

Inglés Hablado: Avanzado, Escrito: Avanzado

Disponibilidad p. viajar No