o Supports and collaborates with the project team for validation efforts right from inception, design build, test and implementation

o Investigate/troubleshoot validation discrepancies for systems and/or performance processes

o Support validation activities – IQ/OP/PQ

o Support ethylene oxide requalification activities to meet ISO requirements on time

o Create change controls and provide assistance in determining root cause for non-conforming events and evaluate CAPAs for effectiveness

o Ensures required processes and procedures are followed to support validation programs and are in compliance with regulations

o Co-operates with all departments through open, candid communication and collaboration

o Prior experience working with ethylene oxide and gamma sterilization processes

o Pharmaceutical Industry GMPs. Interpret & Apply ISO 11135, 11137, TIR 15, TIR 28, 11737 and FDA and Country specific guidelines to the

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