In this role, you have the opportunity to
The Process Quality Engineer 3 will work primarily with Philips-Volcano’s 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 responsible for
Provide quality compliance decisions for manufacturing process transfer from other sites, R&D or new implementations as applicable for operations quality engineering. Generate, review and approve the necessary deliverables in all related Quality Systems required to complete these activities.
Review reported manufacturing process problems and determine the best course of action within Volcano’s quality system to address the product or process problem. Execute the necessary actions to bring products and processes back to conformance within the quality system requirements.
Support assigned areas improvement projects (Lean, Yield improvements, Complaint reduction initiatives)
As necessary, performs other duties as required.
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
KNOWLEDGE AND EXPERIENCE:
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 and proven knowledge of Measurement and Test tools (e.g. calipers, micrometers, Coordinate Measuring Machines (CMM), etc) 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, scatter diagrams, regression analysis, affinity diagrams, etc).
Proven knowledge and application of applicable regulations for Medical Device manufacturing.
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.