Provide information and tools to the production area to meet product and process specifications.
Develop new products.
Develop testing.
Participates in process and product decision-making.
Responsible for conducting FMEA and APQP.
Provides quotations for new products.
Optimizes materials for new product development.
Prepares technical information for the manufacture of new products.
Controls and develops engineering changes and engineering reviews.
Qualifications
Bachelor’s degree in engineering Mechanical, Electrical, Mechatronic, Robotics, industrial or similar
English Level: Proficient
Basic knowledge in hydraulic and pneumatic diagrams, interpretation of plans
At least 2-year work experience in a global company of medical devices
Learning agility
Communication skills
Teamwork
Results oriented
Easy to adapt
Strong leadership skills
Equal Employment Opportunity
Experience in ISO 13485 and CFR 820 FDA Required
Process validation (IQ,PQ,OQ)
Transfer process of medical devices
Statistical techiques
Risk management ISO 14971
QOPQ
Sueldo: $75,000.00 - $90,000.00 al mes
Ventajas
- Aumentos salariales
- Ayuda o servicio de transporte
- Estacionamiento de la empresa
- Estacionamiento gratuito
- Horarios flexibles
- Opción a contrato indefinido
- Seguro de gastos médicos mayores
- Seguro de vida
- Servicio de comedor
- Vales de despensa