Quality engineer ii -medical industry-

794232

Salario confidencial CRC

Toda Costa Rica

Publicado 17 Sep 2020

Aseguramiento de calidad

2 Vacantes

Ingeniería Eléctrica - Electrome... / Otras


Sector de la vacante:
Industrias manufactureras

Descripción general

Responsibilities:
• Validate new equipment, products or processes. Prepare, run, and analyze data for IQ, OQ, PQ, SQ, TVM, and FMEAs protocols and reports.
• Train operators and engineers in validation activities.
• Investigate customer complaints, suppliers and internal nonconformities. Conduct root cause investigations, determine corrective action, and verify effectiveness.
• Develop / analyze statistical data and product specifications to determine manufacturing quality standards.
• Approve customer drawings for use in manufacturing.
• Create and modify current procedures and instructions.
• Prepare / present technical information and quality metrics to team members, clients and management.
• Serve as a liaison professional with external clients.
• Maintain practical knowledge of government standards and industry quality assurance standards.
• Develop internal audits to ensure compliance with applicable regulatory standards / requirements and organizations and ISO.

Requisitos para aplicar

Education and Experience:
• Title that accredits you for the performance of the position in Engineering areas or an equivalent discipline.
• Desirable CQE / CSSBB certification.
• 3-5 years of experience in similar positions.
• Fundamental understanding of geometry, fractions, percentages, relationships, and measurements.
• Complete understanding of administrative and manufacturing processes.
• Interpersonal skills and adaptation working with employees from different cultures.
• Ability to read / interpret procedural materials such as job travelers, plans, sketches, and diagrams.
• Excellent technical procedure writing skills.
• Excellent verbal and written communication skills between departments.
• Expert in the application of inferential statistics (Minitab, JMP)
• Previous experience working with a driven standard (ISO, FDA, etc.)
• Knowledge of Computing with inventory and manufacturing software, order processing systems, spreadsheets and word processors.
• Skills organizing effective time, applied to fast movements and high pressure environments.
• Ability to work independently with little or no supervision, as well as in work teams.

Datos complementarios

794232

Profesional

Ingeniero / Otras

Bachillerato universitario

Equipo medico

5 años de experiencia

794232

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