Rob Hughes
Rob Hughes has
worked in the pharmaceutical industry for more than 35 years.
Rob started
his career in control laboratories before gaining accreditation as a “Qualified
Person”.
During his
career, he has held operational, project and senior strategic
leadership positions in commercial manufacturing and development QA. Rob has
experience of the application of quality assurance in control laboratories,
active substance, solids, creams and liquids manufacture, supplier evaluation
and in regulatory inspections.
In the
strategic roles, Rob was responsible for the leadership of global groups, which
developed and rolled out quality systems across the company network of sites.
Rob spent two
years in R&D project management with a focus on the reduction of
development timelines, prior to establishing his consultancy in 2012.
Since then,
Rob has worked with many different companies in the development, remediation
and implementation of quality systems, training of staff from operator to
management level and auditing of quality systems.
An Introduction to Quality Management for Managers
15 Sep 2022
This seminar has been designed to provide a highly interactive introduction to Quality Management for managers and will provide the opportunity to share and consolidate the key elements of the Pharmaceutical Quality System (PQS). It will provide practical advice and guidance on how to ensure legal and operational responsibilities are fulfilled.
Quality Management Refresher
29 Sep 2022
This seminar has been designed to provide a highly interactive session to refresh key personnel in the principles and practices of Quality Management and bring them up-to-date with the latest legal requirements. The seminar will review the key elements of the Pharmaceutical Quality System (PQS) and the roles and responsibilities of all staff involved in the PQS, including management.
It will also provide a comprehensive overview of the essential principles and requirements of "The Orange Guide” and other relevant regulatory requirements.
GMP Fundamentals
18-19 Oct 2022
This two-day seminar will consider the relationship between the legal requirements for pharmaceutical manufacture, the PQS and the delivery of GMP. It will provide a highly interactive session to discuss the key elements of the PQS and the relationship with GMP as described in the “Orange Guide”, including the practical application of GMP in manufacturing and quality control.
An Introduction to Quality Management for Managers
13 Dec 2022
This seminar has been designed to provide a highly interactive introduction to Quality Management for managers and will provide the opportunity to share and consolidate the key elements of the Pharmaceutical Quality System (PQS). It will provide practical advice and guidance on how to ensure legal and operational responsibilities are fulfilled.
Quality Management Refresher
26 Jan 2023
This seminar has been designed to provide a highly interactive session to refresh key personnel in the principles and practices of Quality Management and bring them up-to-date with the latest legal requirements. The seminar will review the key elements of the Pharmaceutical Quality System (PQS) and the roles and responsibilities of all staff involved in the PQS, including management.
It will also provide a comprehensive overview of the essential principles and requirements of "The Orange Guide” and other relevant regulatory requirements.