Quality Engineer - Document Control & Software Testing

Lifoam Industries LLC; Belgique; Sur place; EUR 45 000 - 65 000; Plein temps

Résumé du poste

Lifoam Industries LLC is seeking a Quality Engineer to manage QMS document control and ensure product quality throughout production. You will organize, maintain, and update quality documents, work closely with development teams to improve product quality, and prevent defects to uphold high standards across the manufacturing process.

The role involves designing test plans, executing manual and automated tests, and coordinating with stakeholders to ensure compliance with ISO, FDA, or CMMI

Qualifications

• Bachelor's degree in CS, Engineering, or related field.
• 2–4 years in quality in manufacturing or software.
• Experience with ISO, FDA, or CMMI standards preferred.

Responsabilités

• Manage and maintain documents within the QMS.
• Review and approve project documents.
• Audit documents for accuracy and compliance.
• Support internal and external audits/ inspections.
• Train staff on document management procedures.
• Design and execute test plans and cases.
• Perform manual and automated software testing.
• Identify defects and collaborate with development.
• Perform root cause analysis and drive improvements.
• Maintain document control databases and systems.

Connaissances

Document control

Test planning

Manual testing

Automated testing

Root cause analysis

Regulatory compliance

Cross-functional collaboration

Quality assurance

Formation

Bachelor's degree in CS/Engineering

Outils

Microsoft Office

QMS administration

Description du poste

Lifoam Industries LLC is seeking a Quality Engineer to manage QMS document control and ensure product quality throughout production. You will organize, maintain, and update quality documents, work closely with development teams to improve product quality, and prevent defects to uphold high standards across the manufacturing process.

The role involves designing test plans, executing manual and automated tests, and coordinating with stakeholders to ensure compliance with ISO, FDA, or CMMI