David AbrahamAn experienced quality professional with a successful career developing, implementing, maintaining and improving business processes and quality management systems, across a varied business portfolio, ensuring compliance to relevant industry regulatory and company requirements, in addition to the management and coordination of various projects from concept to completion.

David has developed a wealth of knowledge in a wide variety of fields across the Pharmaceutical supply chain gaining extensive knowledge of business operations and processes, manufacturing operations, logistics, printed packaging and pharmaceutical industry applications including but not limited to auditing, training, development of plans in QMS maturity, risk and compliance management, change control, process improvement, regulatory compliance and good manufacturing practice (GMP/GXP/GDP etc.)

During his career David has also worked in and alongside working parties at national, European and international level as a subject matter expert in the development of guidance and standards for the industry and has been instrumental in the development of the PS 9000 publications.

Specialisms (Capabilities)

Rules and Guidance for Pharmaceutical Manufacturers and Distributors (Orange Guide). PS9000, PS9004, ISO15378, ISO 9000, ISO14001, ISO13485, ISO27001, BRC/IOP, Risk Management, Business continuity, Health & Safety (18001), EN15823 Braille on packaging, TQM, Error Prevention Systems,  in addition to other ISO application standards

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