Job Opportunities in Costa Rica
September 27, 2024
Philips
Alajuela
Quality Inspector Supervisor 3
Job Title
Quality Inspector Supervisor 3Job Description
Quality Inspector Supervisor 3
Role Overview
The Quality Inspection Supervisor will work directly with manufacturing and production departments to coordinate QPIs/QA Tech support required to activities for continued operation of the manufacturing lines of Costa Rica site.
The Quality Inspection Supervisor will also be assigned improvement or remediation project activities in support of the organization’s needs for continuous improvement or maintenance of regulatory compliance in areas under his/her responsibilities.
Lead a group of direct report (Quality Inspectors (QPIs) and Quality Technicians (QA Techs)) as required.
You are responsible for
To succeed in this role, you’ll need a customer-first attitude and the following
The Quality Inspection Supervisor will work directly with manufacturing and production departments to coordinate QPIs/QA Tech support required to activities for continued operation of the manufacturing lines of Costa Rica site.
The Quality Inspection Supervisor will also be assigned improvement or remediation project activities in support of the organization’s needs for continuous improvement or maintenance of regulatory compliance in areas under his/her responsibilities.
Lead a group of direct report (Quality Inspectors (QPIs) and Quality Technicians (QA Techs)) as required.
You are responsible for
- Ensures that the quality system is in place, for the ongoing manufacturing process, that include all stages of the manufacture of the product/system.
- Oversees processes: trend analysis, PPM, Sigma level among others
- Ensures a good defect criteria for the QPIs.
- Ensures correct supervision of the QPIs personnel.
- Ensures correct development of the lot release process.
- Apply the correct GMPs methodologies.
To succeed in this role, you’ll need a customer-first attitude and the following
- Bachelor's degree in a Technical, Science, or Engineering discipline strongly preferred or Equivalent years of experience in manufacturing industry.
- Requires at least 5 + years’ experience in the medical device industry or regulated industry
- Requires at least 5+ years’ experience lead people
- Fluent English skill spoken and written.
- Ability to interpret and manage technical drawings that may include mechanical dimensioning and Geometric Dimensioning and Tolerance (GD&T) is preferred.
- 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).
- Basic understanding of an IQ/TMV.
- Experience in document change control.
- Knowledge in NCRs development, Knowledge of the CAPA process.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
- Learn more about our business.
- Discover our rich and exciting history.
- Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
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