**MUST HAVE EXPERIENCE IN THE MEDICAL DEVICE INDUSTRY WITH VALIDATIONS PROTOCOLS (IQ, OQ, PQ)**
**KEY RESPONSIBILITIES**:
- Provide technical engineering support for validations, may write Installation Qualification (IQ) validation protocols, execute validation activities, and provide data to write completion reports for assigned validations.
-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 basic 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.
-1 - 3 years of experience in the manufacturing industry and/or 1 year of experience in medical industry
-Good presentation skills before groups/clients.
-Basic knowledge of statistics.
-Intermediate English level (reading and writing) with basic conversation skills
MXOPS
Pay: $****** - $****** per month
Work Location: In person

📌 Ingeniero De Validacion I - 30050 (Ciudad Juárez)
🏢 Bepc
📍 Ciudad Juárez