12 publicaciones de empleo destacadas en data engineer ii, dash device (¡Están contratando!)

Quality Engineer II
Steris —Guadalupe, N. L.
- Tiempo completo
- Ensamblaje
- Licenciatura
- Mejora continua
Supplier Quality Engineer H/F
Amphenol TCS de México S.A. de C.V —Mexicali, B.C.
- Administración de personal
- Inglés
- Licenciatura
Postulación rápida
Security Analyst
Intuitive Surgical —Mexicali, B.C.
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Equipment Technician
Intuitive Surgical —Mexicali, B.C.
- CAD
- Inglés
- Microsoft Office
3d
Automation Manager H/F
Amphenol TCS de México S.A. de C.V —Município de Mexicali, B.C.
- Administración de personal
- Inglés
- Ensamblaje
Postulación rápida
Regulatory Postmarket Specialist
Intuitive Surgical —Mexicali, B.C.
- Doctorado
- Análisis de datos
- Inglés
10d
Import Export Supervisor
Intuitive Surgical —Mexicali, B.C.
- Microsoft Excel
- ERP systems
- Inglés
Senior Software Engineer– Salesforce Full Stack Developer
Salesforce —Ciudad de México, CDMX
- Tiempo completo
- DevOps
- SQL
- JavaScript
Import Export Supervisor
Intuitive —Mexicali, B.C.
- Tiempo completo
- Microsoft Excel
- ERP systems
- Inglés
Postulación rápida
Director, Accounts Payable & Travel Expense
Intuitive Surgical —Mexicali, B.C.
- Oracle
- Administración de personal
- ERP systems
Supply Chain Program Manager I
Regal Rexnord —Baja California
- Tiempo completo
- Microsoft Excel
- Administración de personal
- Licenciatura
5d
FBS Data Product Owner III
Capgemini —México
- $1 por año
- Tiempo completo
- Home Office (Desde casa)
- Azure
- Administración de personal
- SQL
- Vacaciones adicionales o permisos con goce de sueldo
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Proven project management experience (3–4 years preferred). Manage communication with OEMs, suppliers, and internal/external stakeholders.
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Quality Engineer II

Steris -
Guadalupe, N. L.

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Información del empleo

Tiempo completo

Cualificaciones

Ensamblaje
Licenciatura
Mejora continua
Experiencia en manufactura

Descripción completa del empleo

Position Summary

The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR, NOM-241-SSA1, ASME Sección VIII division 1 and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems.

Duties

Participate on cross-functional new product development teams with focus on product/ service quality and Quality System compliance.
Develop and implement statistically valid sampling plans, designed experiments, capability studies, SPC and trend analysis.
Initiate and/or participate in process and product corrective actions and problem-solving activities.
Update/establish documented work instructions as needed.
Review collected data to perform statistical analysis and recommend process/product changes to improve quality.
Monitor and report on performance metrics.
Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
Collaborate with other departments and facilities within the company on quality related issues.
Maintain product integrity and quality through support of evaluation and disposition of nonconforming materials.
Perform quality system audits and provide guidance on corrective actions.
Perform other duties as assigned
Compliance FDA and ISO 13485
Non-destructive testing (NDT) according to CSEI (AQSIQ
ASME and PED code activities.

Education Degree

Bachelor's Degree in Engineering General

Required Experience (3 years)

Combined Manufacturing/Quality Engineering/Quality Systems experience or minimum of 6 months on-site STERIS internship or co-op experience.
Working in an ISO certified environment required.
Medical device or other regulated industries experience preferred.
ASQ, QSR or familiarity with QSR/GMP regulations
Demonstrate experience leading or participating on improvement projects
Background on steel, mechanic assembly process.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.

STERIS strives to be an Equal Opportunity Employer.

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data engineer ii, dash device empleos

Quality Engineer II

Supplier Quality Engineer H/F

Security Analyst

Equipment Technician

Automation Manager H/F

Regulatory Postmarket Specialist

Import Export Supervisor

Senior Software Engineer– Salesforce Full Stack Developer

Import Export Supervisor

Director, Accounts Payable & Travel Expense

Supply Chain Program Manager I

FBS Data Product Owner III

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Position Summary

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Required Experience (3 years)

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