Tecate, Baja California- Beneficios de acuerdo a la LFT
- Fondo de ahorro
- Transporte
- Utilidades garantizadas
- Servicios medicos en planta
- Comedor
- caja de ahorro
- comedor
- fondo de ahorro
- servicios médicos en planta
Corporativo
Giro
Maquiladora (Export.)
Actividad principal
Manufactura de dispositivos medicos diversos.
Número de empleados
750
Sitio Web corporativo
Sitio Web
Descripción y detalle de las actividades
- Plans and leads process development activities including design, prototyping, testing (verification and validation) risk management/process FMEA, process characterization, and documentation. Participate in the redesign of existing processes to improve quality, utilize automated production techniques, optimize process capabilities, and product improvements in a more cost-effective manner.
- Provide technical expertise in developing new assembly tooling, guidance in processing and troubleshooting.
- Interface with new product development and manufacturing to understand product requirements and establish design criteria for manufacturing processes.
- Interact with suppliers to define and evaluate materials and processes needed for effective execution of process development activities.
- Responsible for validations, IQ/OQ/PQ, product production within agreed upon scope, budget, timeline, and quality.
- Interact with suppliers to debug problems with production parts, processes and equipment.
- Interface with procurement to obtain quotations, purchase components.
- Advise other engineering personnel on technical aspects of product/process design, assembly techniques and the validation of processes.
- Interface with engineers, manufacturing, and lab technicians to design and develop new fixtures and tooling.
- Support product related technical problems in engineering and manufacturing areas.
- Develop comprehensive manufacturing strategy for all projects that will include alternate methods for component acquisition including timelines, costs, capital, expense, risk, and recommendations
- Interface with suppliers and manufacturing when implementing new processes.
- Coordinate with SBU planning for initial and ongoing supply, safety stock, distribution management including shelf life, and alternate suppliers for critical components
- In conjunction with Quality establish AQL levels for each component and incoming inspection criteria including location, method of measurement, consistent data recording, disposition.
Experiencia y requisitos
- Bachelor level degree in engineering
- 3+ years previous experience in related field (e.g., medical device manufacturing and assembly, disposables manufacturing processes, plastics, automation).
- Strong bilingual (English/Spanish) communication and presentation skills (written and verbal).
- Ability to work effectively with other product development team members.
- Experience in the medical industry / Knowledge of ISO 13485.
*** The site to work is in Tecate Site.
Beneficios
Número de vacantes 1
Área Ingeniería
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Disponibilidad p. viajar Si