An experienced QP specialising in Good Manufacturing Practice (GMP), Sue has been a fixture within the pharmaceutical industry for more than 40 years and has worked across multi-nationals, contract manufacturing and virtual platforms.
Having run her own consultancy since 2009, Sue works with companies from around the world, advising on best practice and developing, enhancing and/or simplifying their operations.
A Qualified Person (QP) since the mid-1980s, later becoming a QP Assessor in the early 2000s, Sue understands the complexity of this challenging role and its position within a company. She applies this knowledge, using real life scenarios, to several of our QP modules.
Sue has both commercial and R&D experience working with IMPs, including packaging and labelling for double blind trials. In addition, she has worked with most major dosage forms including oral solid dose, liquids and semi solids and sterile products.

Sue is skilled and well sought after when it comes to developing and/or simplifying Pharmaceutical Quality Systems (PQS) so they are effective and efficient. She has a good record of dealing with post regulatory inspection issues at sites with positive inspection afterwards.
With core knowledge in GMP, Sue has assisted the WHO and has been involved in a development project in several African countries, funded by UNIDO. Sue has also acquired Good Distribution Practice (GDP) experience and has helped write a guidance document published by PQG and ECA which expands upon the EU GDP Guideline.
An inspiring trainer, Sue can break down complex topics into understandable elements and can provide appropriate training to all career levels.