Job Description

**Descripción y detalle de las actividades**:
- Communicates and provides essencial information to the Quality Systems Supervisor.
- Establish and maintain a configuration management system compliant with regulatory, quality, company and customer (both internal and external) requirements.
- Collaborate with cross-functional departments to ensure timely implementation of change requisitions and change orders.
- Document and generate in Quality system the approved templates of manufactured product.
- Maintain files of official recorded documents, archive and label documents for permanent storage in the vault,
- Have communication and coordinate needs with departments.
- Responsible for reviewing procedures and facilitating procedures updates in the assignment process.
Experiência y requisitos:
- University certifcate completed.
- Required a minimum of 2 years of experience in quality areas or similar, preferably focused on medical manufacturing produc inspec...

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