Paul Irving

Principal Consultant

Northern Life Sciences Ltd


Paul Irving has extensive experience as a compliance and validation consultant in the life sciences industry. He specializes in information governance, data integrity program set up and implementation, and computerized systems validation. While working at Kimberly-Clark, Paul also gained experience in all aspects of quality control, including statistical process control and development of management information systems. In recent years, he has led large programs of quality and compliance transformations for leading biotechnology organizations.  Currently, Irving operates as a Strategic Consultant for Northern Life Sciences Ltd. within the UK, US, and CEE. Paul has also worked extensively in Eastern Europe, working on many key strategic Life Sciences Organisation Digital Transformation Programs and Travels to Poland frequently.  He has been an International Society of Pharmaceutical Engineering (ISPE) member since 2001, serves on the GAMP® EU Steering Committee, was formerly Co-chair of the GAMP® Special Interest Group on Manufacturing Execution Systems, and has contributed to various GAMP® guidance documents, including Chapter Lead for GAMP® 5 Second Edition Electronic Production Records.  Co Author MES GAMP® Guide for Industry, Part of CORE TEAM who authored ISPE GAMP® RDI Manufacturing Records Guide for Industry, he is also a Recognised International Trainer and Industry Speaker.

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