Mexicali, Baja California- Beneficios Superiores a LFT
Correo de contacto
*****@masimo.com
Giro
Maquiladora (Export.)
Actividad principal
Ensamble de sensores para oximetros (productos médicos).
Número de empleados
4350
Sitio Web corporativo
Aviso de privacidad
Descripción y detalle de las actividades
- Develop and implement documents applicable to the Quality inspection
- Ensure, through training and verification, the appropriate use of current documentation, as well as the use of good documentation practices during all the stages of manufacturing.
- Ensure and monitor the applicable documents for Quality inspection are available in the point of use, this includes, but is not limited to the visual aids with physical samples.
- Coordinate Inspection activities and product release for further processing, in all areas.
- Ensure that inspection procedures are to the latest revision.
- Ensure that acceptance criteria is met and updated.
- Ensure that product status is clear during all the stages of the manufacturing process.
- Support in New Product development and validation, generating Acceptance Procedures and Quality Documents (new documentation)
- Ensure that all Equipment that requires calibration, is calibrated.
- Ensure that procedures related with quality responsibility are updated
- Make sure DHRs are reviewed and closed on time per applicable procedures.
- Participate in the MRB process and follow up actions in order to reduce non conformances.
- Manage Quality Control Inspectors and/or Technicians
- Perform Quality System activities such as: PDA process, Internal Audits, Internal Observations, Document Control and Analysis of Data.
- Overall coordination, tracking/status of all in-house MRB material..
- Maintains and comply Quality metrics.
- Supervise nonconforming storerooms: Transfers, Acceptance Status, Storage Requirements, Material Requests, Cycle counts, Housekeeping
- Performs other duties or special projects as assigned
- Coordinate RMA processing (receiving, investigation, repair, and delivery).
- Conduct internal audits, document and communicate findings, and create
- audit records.
- Work with departments/auditees, OBS and CAPA owners to address identified issues, assisting owners and team to find root cause using statistical techniques.
Experiencia y requisitos
- Advanced English
- 3+ years of experience as a Quality Engineer in the medical device, aerospace, or automotive industry.
- Direct experience in Quality System Audits.
- Root Cause investigation, failure analysis and developing robust corrective and preventive actions.
- Carries out both routine and moderately difficult assignments with minimal supervision
- Competent in all company quality system procedures and practices
- Carries out projects independently and/or completes assigned tasks for major projects.
- Performs routine In process audits to the manufacturing floor and Quality areas.
- Ability to analyze situations thoroughly, identify potential problems, find and implement effective solutions
- Hands on experience implementing and using statistical methods throughout various aspects of product realization, including but not limited to the use of Minitab, PFMEA, DOE and Gage R&R methodologies
- Developing quality control systems.
- troubleshooting skills
- Developing and implementing quality standards.
- Monitoring and analyzing quality performance.
- Inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met.
- Collaborating with operations managers to develop and implement controls and improvements.
- Ensuring that workflows, processes, and products comply with safety regulations.
Beneficios
Número de vacantes 1
Área Calidad
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
Horario
- Monday to Friday 08:00-17:30 hrs
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Disponibilidad p. viajar No