| Área de la Empresa | Manufacturas Varias |
| Cargo Solicitado | Otros empleos |
| Puestos Vacantes | 1 |
| Tipo de Contratación | Tiempo completo |
| Nivel de Experiencia | Sin experiencia |
| Salario máximo (USD) | |
| Salario minimo (USD) | |
| Vehículo | Indiferente |
| País | República Dominicana |
| Departamento | Otro |
Job Summary:**
The Validation Technician at Jabil, Inc. performs essential validation activities to ensure manufacturing processes, equipment, and products meet established quality and regulatory standards. This role supports the production of high-quality medical devices and other regulated products.
Job Responsibilities:**
* Execute validation protocols (IQ, OQ, PQ) for equipment, processes, software, and cleaning procedures in accordance with company policies and regulatory requirements (e.g., FDA, ISO 13485).
* Perform testing, data collection, and analysis during validation activities, ensuring accuracy and completeness of results.
* Document all validation activities thoroughly, including deviations, corrective actions, and final reports.
* Support the development and review of validation protocols and reports.
* Conduct routine calibration and maintenance of validation equipment and instrumentation.
* Identify and troubleshoot issues during validation runs, escalating complex problems to engineering or management.
* Assist in the investigation of non-conformances and deviations related to validated processes.
* Maintain accurate and organized validation documentation and records.
* Collaborate with engineering, quality, and production teams to ensure successful validation project completion.
* Adhere to all safety guidelines and company policies.
Job Qualifications:**
* Term-student or graduated in a scientific, engineering, or technical field, or equivalent experience.
* 1-3 years of experience in a regulated manufacturing environment (e.g., medical device, pharmaceutical), with specific experience in validation preferred.
* Familiarity with Good Manufacturing Practices (GMP) and relevant regulatory standards (e.g., FDA 21 CFR Part 820, ISO 13485).
* Strong attention to detail and accuracy in data collection and documentation.
* Excellent written and verbal communication skills.
* Ability to read and interpret technical documents, blueprints, and schematics.
* Proficient in using standard laboratory equipment and measurement tools.
* Basic computer skills, including Microsoft Office Suite.
* Ability to work independently and as part of a team.
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