Your role will be responsible for ensuring that the WFI and Clean Steam Systems meet the quality and compliance criteria of regulatory agencies.

Within this role you will:

• Generation of Protocols IQ/OQ & PQ
• Construction/Equipment Dossiers Reviews
• Ensure high standard of cGMP documentation is compliant with regulations and corporate standards
• Assist in the development of Sampling schedules
• Review quality system SOPs
• Review Corporate Standards
• Execution of Qualification Proctocols
• Generation of Final Reports.

To be successful in this role you will require:

Engineering qualification,

Min of 3 years of relevant work experience in validation of clean utility systems in the pharmaceutical industry.

Experience of sterile manufacturing within the pharmaceutical industry would be a decided advantage

Knowledge of GMP, safety and environmental regulatory requirements