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