Quality Engineer (Mexicali)
Link-Worldwide
Detailed daily activities
- Review new and modified processes.
- Analysis for validation or revalidation requirements (IQ/OQ/PQ).
- Validation protocols creation.
- Validations tracking.
- Support on validation corrective actions required.
- Report validation results.
Statistical support on production processes
- Required SPC tool evaluation.
- Report validation results.
- Capability studies implementation.
- Gage R&R; implementation.
- Support to implement methods/altern sampling.
- Support to eliminate destructive tests.
- Support to improvement projects.
Job Requirements
Experience
- Industrial Engineer, Mechanical Engineer, Electronics Engineer, or similar.
- Medical Industry Experienced.
- QMS and ISO Standard Knowledge (ISO13485 and/or FDA GMP).
- Manufacturing Process 3-year-experienced.
- New Product development/Process transfers/Process improvement experienced.
- English about 85% Preferred (spoken, written, read).
Operating Company
Ormco
#J-18808-LjbffrVacante publicada el 14 horas atrás
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