Ingeniero De Calidad Sr

Tacna; Tijuana; On-site; MXN 900,000 - 1,300,000; Full time

Job summary

Vapotherm, Inc. busca un Ingeniero/a de Calidad Senior para representar la calidad en proyectos y brindar soporte a la producción y operaciones mediante la implementación del Sistema de Gestión de Calidad de Vapotherm.

Responsable de apoyar funciones de calidad, revisiones de validaciones, documentación de procedimientos y mejoras continuas para garantizar un rendimiento óptimo y entrega segura al paciente. Se requiere dominio de ISO 13485 y ISO 14971, así como experiencia en entornos regulados.

Qualifications

• Se solicita título en Ingeniería o Ciencias.
• 5–10 años en fabricación de dispositivos médicos o industria regulada.
• Enfoque en calidad orientado al paciente/cliente.
• Conocimiento de ISO 13485 y ISO 14971.
• Conocimiento de técnicas estadísticas.
• Experiencia con software de hojas de cálculo, bases de datos y procesamiento de texto.

Responsibilities

• Participar en la ejecución de funciones de calidad conforme a FDA QSRs, ISO 13485 e ISO 14971.
• Revisar y validar verificaciones/validaciones de procesos (IQ/OQ/PQ) y documentar informes.
• Colaborar en actualización de documentación de procedimientos y trabajo.
• Apoyar gestión de riesgos en procesos de manufactura (pFMEA).
• Redactar o actualizar procedimientos para mejora de procesos.
• Investigar materiales no conformes y oportunidades de mejora en manufactura y producto.
• Apoyar auditorías de proveedores y auditorías internas/externas.

Skills

Inglés fluido

Español fluido

Education

B.S. en Ingeniería o Ciencias

Tools

Excel

Bases de datos

Procesadores de texto

Job description

Vapotherm, Inc

Descripción y detalle de las actividades

Position Title: Senior Quality Engineer Reports To: Quality Leadership Department: RA/QA Summary of Position (Paragraph form): The Quality Engineer will be responsible for representing quality on projects, overall quality support to the production and operations organization including implementation of Vapotherm’s Quality Management System.

Primary Responsibilities (Bulleted form):

• Participate in the execution of Quality functions in compliance with FDA QSRs, ISO 13485, ISO 14971, and other national and international quality requirements and standards.
• Assists in reviewing and executing process verifications and validations, including IQ/OQ/PQ protocol and report documentation.
• Cross-Functional team member assisting in preparation and updates of manufacturing procedure documentation.
• Support risk management activities related to manufacturing processes such as pFMEA.
• Review and assist in writing new procedures and work instructions or updating existing documents to drive process improvement.
• Evaluate and monitor manufacturing issues, and product concerns, and help investigate non-conforming material to determine opportunities for improving manufacturing and product performance.
• Support supplier related activities, such as supplier audits, manufacturing validation, and proposed changes.
• Performs internal audits and assists in hosting external audits.

Position Requirements - Education, Knowledge, Years of Experience, etc. (Bulleted form):

• B.S. in Engineering or Science, or equivalent technical field.
• 5-10 years in Medical Device Manufacturing or other regulated industry.
• Patient/Customer Focused Quality perspective.
• Working knowledge of QMS standards like ISO 13485 and familiarity with Risk management standards like ISO 14971
• Working knowledge of statistical techniques.
• Working knowledge in spreadsheets, databases, and word processing software programs.
• Strong attention to detail.
• Highly organized.
• Fluent in English and Spanish
• Effective written and oral communication skills.
• Ability to work as a team or independently in a changing, fast-paced, deadline-driven environment; must be driven and able to accept new challenges and continually strive for improvement in the support of effective therapy delivery to the patient and a delighted user experience.
• Employ an engaged, collaborative mindset with teammates within the RA/QA department, as well as during frequent project interface with interdepartmental (Manufacturing Engineering, Production) colleagues.
• Must have experience with and demonstrable competencies in Lean Manufacturing (e.g. Toyota Production System). Including leading Kaizens/Continuous Improvement techniques, Standard Work, Single Piece Flow, Kan Ban, 5S, SMED, Value Stream Mapping, and Poka Yoke

Informacion de la empresa

No especificado

Información Extra Vacantes Abiertas 1 Turno L-J:7:00-17:00, V:7:00-15:00 City Tijuana IdiomasEnglish (80 %)
DocumentosSin especificar