Job Description

Descripción y detalle de las actividades
- Maintain Quality Records in appropriate location.
- Capture Training logs/roster for the site.
- Training Data base handling.
- CAPA facilitator.
- Responsible to archive quality records (Training files, Logs, TCR, etc).
- Audit/verify documents are compliant with GDPs.
- Responsible for the distribution of controlled copies and retrieval when needed.
- Assess/Audit of current controlled documents are posted at site level.
- Scan DHR documentation prior to ship product to LLC for digital archiving.
- Prepare records for outside storage (Iron Mountain).
- Responsible for shredding obsolete/unused documents for the site.
- Responsible for the support on document translations.
- Purchase appropriate consumables for records shipping.
Experiência y requisitos
- Experience with GMP and GDP, Clean room environment.
- Medical device manufacturing environment.
- Ability to communicate effectively inter...

Ready to Apply?

Take the next step in your AI career. Submit your application to Sonova today.

Submit Application