Validation Engineering

Descripción del Empleo:
The Validation Engineer will work with our Clients and be responsible for preparing and executing validation documents. Demonstrate an understanding of cGMP. Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management and peers.
Essential Duties include, but are not limited to:
Develop Validation Master Plan (VMP)
Develop process validation protocols (IQ, OQ, PQ) for Automated Equipment.
Develop Manufacturing Standard Operating Procedures.
Develop Test Methods.
Develop Preventive Maintenance Procedures.
Execute and Planning Validation Activities.
Coordinate Equipment Installation and Calibrations.
Develop and system routing of Change Control and Change Request.
Agile system management.
Compile/Analyze analytical validation data and test results.
Requisitos:
Bachelor's degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Industrial Biotechnology or related sciences.

-Minimum of 3-5 years of experience in pharmaceutical and medical device industry. Full bilingual