Our company is looking for a validation engineer with fair experience in pharmaceutical industry. Your primary responsibility will be to evaluate engineering systems based on safety and performance standards. You’ll analyze results and update activity logs. Troubleshooting and maintaining equipment will also be part of your duties.
If you are organized, detail-oriented and have a fair engineering background, we’d like to take this ahead.
Responsibilities :
~Establish performance and quality criteria
~Understanding the client’s URS
~Complete validation process : DQ/IQ/OQ (for hardware & software)
~Create and run quality tests based on appropriate protocols
~Evaluate engineering systems and processes
~Calibrate and repair systems and machinery
~Prepare and maintain testing equipment
~Keep and update activity logs
`Perform troubleshooting
`Ensure compliance with safety and quality standards
`Collaborate with engineers and technicians on projects
Requirements
~Previous experience ( minimum 2-3 years) as a validation engineer or in a similar role in calibration section.
~Strong understanding of manufacturing processes and safety regulations
~Knowledge of GAMP, WHO , 21 CFR Part11 Guidelines.
~Excellent mathematical and analytical skills
~Attention to detail
~Teamwork skills
~Degree/Diploma in Electrical/Science/Instrumentation/Electronics