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
Work primarily with manufacturing processes 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.
Will be assigned improvement or remediation project activities in support of the organization’s needs for continuous improvement or maintenance of regulatory compliance.
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
Bachelor’s degree in engineering disciplines or related field or a combination of equivalent job experience in related field.
2 year of experience in Quality or Manufacturing or other related fields.
Requires 2+ years’ experience in the medical device industry or regulated industry
Ability to interpret technical drawings that may include mechanical dimensioning and Geometric Dimensioning and Tolerance (GD&T).
Knowledge of methodologies for inspection test tools is preferred
Knowledge of statistical methods and the use of standard quality tools (e.g. flowcharts, Pareto charts, cause and effect diagrams, control charts).
Understanding and training in applicable regulations for Medical Device manufacturing or equivalent regulations (Food, Electrical Industries or ISO).
Shift B : Monday to Friday : 3 : 36 pm to 10 pm and Saturday 7 : 00 am to 3 : 00 pm
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.