Welch Allyn de Mexico, S. de R.L. de C.V.

Quality Leader

Welch Allyn de Mexico, S. de R.L. de C.V.

Hace 8 horas

Tijuana, Baja California

Giro

Maquiladora (Export.)

Actividad principal

Manufactura de instrumental médico de diagnóstico.

Número de empleados

990

Sitio Web corporativo

Dirección

Emilio Flores 2471-A

Colonia o fraccionamiento

Cañon Del Padre Blvd. Teran Teran

Ciudad

Tijuana, Baja California

Descripción y detalle de las actividades

ESSENTIAL DUTIES AND RESPONSIBILITIES -Achieves quality assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements; implementing change. -Meets quality assurance financial objectives by estimating requirements; preparing an annual budget; scheduling expenditures; analyzing variances; initiating corrective actions. -Maintains and improves product quality by completing product, company, system, compliance, and surveillance audits; investigating customer complaints; collaborating with other members of management to develop new product and engineering designs, and manufacturing and training methods. -Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. -Acts as responsible for servicing Quality Assurance on validation (protocol writing and reporting), master planning of process transfer validation, DOE for process improvement, incoming quality inspection, test and reports, test design, destructive test reduction, among others. -Contributes to attainment of CAPA objectives on his/her assigned areas. -Responsible to direct and guide the Quality Engineers & techs to ensure process control activities including Identification, review and validation of process changes prior to implementation using appropriate tools (CTQs identification, process flow, PFMEA, process validation and process monitoring, etc) to ensure delivey of stable and controlled process to operations. -Develop and train personnel on: complaint investigations, CAPA real root cause fixing, pFMEA Prep., GMPs, GDPs, GLPs training and coaching, NCMR handling and solution, with a risk management approach.

Experiencia y requisitos

EDUCATION, EXPERIENCE, QUALIFICATIONS AND SKILLS: • 5-7 years of experience in the field of Quality Assurance. • Minimum of 2 years of managerial experience. • Proficient and knowledgeable in all areas related to the Quality Assurance function. • Strong knowledge on quality tools (APQP, MSA, SPC, PPAP) • Working knowledge of Statistical Process Control and PCB assembly process, results orientated attitude, achieve through team concept skills / activities. • Strong knowledge of ISO-13485 standards and FDA. CQA, CQE, CSSGB preferiblemente. CQA, CQE, CSSGB preferably. • Bilingual: Oral and written communications in English intermediate

Número de vacantes

1

Área

Control de Calidad

Contrato

Permanente

Turno

Diurno

Jornada

Tiempo Completo

Estudios

Titulo Profesional

Inglés

Hablado: 90%, Escrito: 90%

Sexo

Indistinto

Edad

18 - 65 años