Haemonetics México Manufacturing S. de R.L. de C.V.

Quality Systems Engineer

Haemonetics México Manufacturing S. de R.L. de C.V.

Hace 21 horas

Tijuana, Baja California

Giro

Maquiladora (Export.)

Actividad principal

Líder global en el diseño y fabricacion de productos para la administración de sangre

Número de empleados

1200

Sitio Web corporativo

Dirección

Colinas 11731

Colonia o fraccionamiento

Parque Industrial El Florido ( Secc. Colinas)

Ciudad

Tijuana, Baja California

Descripción y detalle de las actividades

Summary: Responsible for developing and ensuring implementation of quality systems, procedures, test methods, problem definitions and resolutions for existing and new products. Principal Responsibilities: • Assists in manufacturing quality systems, product quality and customer quality requirements. Supports product improvement projects (validation IQ, OQ, PQ activities) and supplier changes to ensure qualification are met. • Completes or may lead teams/projects related to Complaint investigation, CAPA, cost reduction, and quality system excellence. Use of TQM tools including six sigma may be required. • Conducts risk analysis as needed. Conducts internal or external audits as assigned to ensure compliance to company quality system requirements. • Develops, reviews and challenges existing quality driven test systems and procedures to assure products meet intended use. • Key contributor in the design review of new or modified products. Challenge design assumptions to assure design intent manufacturability and customer acceptance levels are achieved and in compliance with Haemonetics SOPs and regulatory standards. • Maintains records to ensure compliance to GMP/ISO requirements. Apply now: https://haemonetics.wd5.myworkdayjobs.com/HAE/job/Tijuana-Mexico/Quality-Systems-Engineer-II_R4078 or send your resume

Experiencia y requisitos

Candidate Education: Required Bachelor's Degree Engineering or Life Science discipline or related technical field Candidate Experience: Required 3 years Work experience Required 3 years Quality experience in the medical device industry Required Other Statistical Process Control experience Candidate Skills: Licenses and Certifications: Required Computer knowledge and experience with Microsoft Office Preferred Six Sigma certification Bilingual (Spanish/English)

Número de vacantes

1

Área

Control de Calidad

Contrato

Permanente

Turno

Diurno

Jornada

Tiempo Completo

Horario

Diurno

Estudios

Titulo Profesional

Inglés

Hablado: 85%, Escrito: 85%

Sexo

Indistinto