Manufacturing Engineer

hace 3 días

Mexicali, México Emprego MX A tiempo completo

Descripción y detalle de las actividades

Purpose of the Job: is responsible for supporting production activities in the medical device industry including yield improvement initiatives, product disposition, continuous improvement activities, assembly procedure development, and process validations. Additional responsibilities will include the transfer of new products and processes into manufacturing, process optimization, mistake proofing, process risk analysis, design reviews and provide input on design for manufacturing. Key Tasks & Responsibilities: Participate and execute validation strategy. -Create, write and execute process validations. -Write and execute process validations. -Lead Projects with some supervision. -Support and lead continuous improvement activities and yield improvement initiatives. -Develop, update pFMEA. -Support production on non-conformances, determine root cause and develop solutions. -Write technical reports. -Experience in developing and implementing production processes (preferred) -Experience in developing tooling and fixtures to support production (preferred) -Experience with micro assembly and electronic manufacturing (preferred) -Experience with equipment specification, equipment troubleshooting and validation (preferred) -Experience with processes such as Laser Welding, Resistance Spot Welding, Automated processes, etc. (preferred)

Experiência y requisitos
- Bachelor's Degree in appropriate engineering field of study or equivalent work experience. Mechanical engineering or related Science. -English Spoken 80% Written 80% -2-5 years’ experience as a manufacturing or mechanical engineering in the medical device industry. -Proven ability to work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence -Self-motivated, decisive, with the ability to adapt to change and competing demands -Flexible with proven ability to conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities -Strong verbal and written communication skills -Strong ability to collaborate in teams and directly with other -Strong interpersonal skills -Strong experience with process validation - IQ, OQ, PQ -Familiarity with processes such as FMEA, CAPA and Standard Works. -Good overall theoretical knowledge of mechanical engineering. -Proficient in Microsoft office, Word, Excel, PPP, Outlook & PLM -Experience with CAD

Organización

Sonova

Correo de contacto

Giro

Manufacturera

Actividad principal

Proveedor de soluciones de cuidado auditivo - Dispositivos Médicos

Número de empleados

800

Aviso de privacidad
- /mexico/es/politica-de-privacidad-de-la-web-y-cookies**Área** Ingeniería

**Contrato** Permanente

**Turno** Diurno

**Jornada** Tiempo Completo

**Estudios** Carrera Profesional

**Inglés **Hablado: 80%, Escrito: 80%

**Sexo** Indistinto

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