Quality Engineer 3
Alajuela, Alajuela, Costa Rica
hace 5 días

Job Description

In this role, you have the opportunity to

Oversees the Quality Assurance in the processes related to the manufacturing of materials, components, sub-assemblies, and completed products and their supply chain, including compliance to regulatory requirements and / or procedures for regulated products / businesses.

The processes include the introduction / validation of new / changed manufacturing processes and their associated Quality systems, the trend analysis and monitoring of manufacturing processes and their environment, the remediation to non-conformances, and the development and improvement of Quality systems.

You are responsible for

The Process Quality Engineer 3 will work primarily with manufacturing processes and engineering counterparts in Advanced Engineering or Design Assurance in support of product inspections, and product and process compliance to established procedures and will take corrective and preventive action as required by procedures to support the continued operation of the Costa Rica site manufacturing lines as well as the introduction of new manufacturing line processes, or transfer of existing processes from other facilities into Costa Rica.

You are a part of

A leading health technology company with a multinational workforce of approximately 77,000 employees and globally present with sales and services in more than 100 countries worldwide.

To succeed in this role, you should have the following skills and experience

Master Degree Desirable.

Requires 5+ years experience in Quality Engineering related activities.

Desirable ability to interpret technical drawings that may include mechanical dimensioning and Geometric Dimensioning and Tolerance (GD&T).

Strong knowledge of Measurement and Test tools e.g. calipers, micrometers and methodologies for inspection (i.e. appropriately apply destructive and non-destructive testing) is preferred.

Strong and proven knowledge of statistical methods and the use of standard quality tools (e.g. flowcharts, Pareto charts, cause and effect diagrams, control charts, regression analysis, etc).

Proven knowledge and application of applicable regulations for Medical Device manufacturing.

Proven ability to understand and interpret established quality system requirements and provide advice to project teams and the organization in general on how to remain compliant to requirements during execution.

In return, we offer you

In order to develop your full potential, we will offer you the flexibility, encouragement and opportunities to keep you inspired and engaged.

After all, working at Philips is more than a job. It is an experience full of amazing moments that will transform you in a lasting and positive way, since together we can improve the world.

Philips is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex (including pregnancy), sexual orientation, gender identity, national origin, genetic information, creed, citizenship, disability, protected veteran or marital status.


Reportar esta oferta

Thank you for reporting this job!

Your feedback will help us improve the quality of our services.

Mi Correo Electrónico
Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
Formulario de postulación