**KEY RESPONSIBILITIES**:
- Provide technical engineering support for validations, write and execute Installation Qualification (IQ) protocols, and provide data to write completion reports for assigned validations.
- Provide technical engineering support for validations, write and execute Operational Qualification (OQ) protocols, and provide data to write completion reports for assigned validations.
- Provide technical engineering support for validations, write and execute Computer Systems Validation (CSV) protocols.
- Provide technical engineering support for validations, write and execute Total Maintenance Validation (TMV) protocols.
- Responsible for running experiments during the pre-validation phase, run other experiments as needed
- Ensure that assigned validation activities are performed in a timely manner and in accordance with current requirements and Good Manufacturing Practices (GMP).
- Demonstrate sufficient knowledge in validation skills, GMP,



Good Documentation Practices (GDP)
- Responsible for the execution of validation, including the creation of forms to create calibration and preventive maintenance records.
**BASIC qualifications**:
- Engineering Degree (master's in science is a plus)
- 3 - 5 years of experience in manufacturing industry and/or 3 - 4 years of experience in medical industry
- Good presentation skills before groups/clients.
- Intermediate knowledge in statistics.
- Intermediate knowledge of Six Sigma, DMAIC and Kaizen.
- Intermediate English level (reading and writing) with intermediate conversation skills.
MXOPS
Tipo de puesto: Tiempo completo
Sueldo: $****** - $****** al mes
Incentivos:
- Seguro de vida
Lugar de trabajo: Empleo presencial

📌 Ingeniero De Validación Iii (Laboratorio) (Ciudad Juárez)
🏢 Bepc
📍 Ciudad Juárez