Speaker Group: Speaker 2022

David Waddington

Dave’s career in the pharmaceutical industry spans 35 years in various Quality roles, most recently as Executive Director with NSF. Dave is eligible to act as a QP and has broad experience in manufacturing, packaging and QC laboratories, including PQS and Regulatory Compliance. He has worked with a wide range of products including medicines, food… Read more »

Ian Holloway

Ian Holloway has extensive experience of GMP, GDP and compliance matters having worked for the MHRA for thirty-five years. He left the Agency in January 2022 as a Senior GMDP Inspector. He managed the Defect Centre and product recall issues for eight years. He was also accredited for GCP and Pharmacovigilance inspections during his time… Read more »

Madeleine Ault

Madeleine is a qualified teacher and former Senior MHRA inspector with prior NHS pharmaceutical manufacturing knowledge. In the role of inspector she was particularly interested in the significance of learning and knowledge sharing and the impact on compliance. Now, as co-director of SeerPharmaUK (https://seerpharma.co.uk), and consultant Responsible Person, Madeleine continues to enjoy meeting industry GxP challenges. Madeleine is part… Read more »

Nina Hauschildt

Nina Hauschildt is a Principal Scientist in the Formulation & Application Services at Evonik Operations GmbH, based in Darmstadt Germany. In this role she gives technical support to customers in North and Western Europe with a focus on excipients for oral drug delivery. She holds a bachelor degree in pharmaceutical engineering and a green belt… Read more »

Wendy Cullen

Wendy has served nearly twenty five years working in the pharmaceuticals industry and has first hand of experience of setting up GMP laboratories and developing analytical services. As a New Product Development Project Manager to Pharmaceutical CMO based in the North of England, Wendy was the interface between the client and the multifaceted production teams… Read more »

Dr Lynne Daintree

Dr Lyn Daintree has extensive knowledge of formulation development using supercritical fluids. Lyn has responsibility for scientific programme management for external client projects, proprietary molecules, compliance, new opportunity assessment and development of intellectual property. Lyn gained her doctorate from the School of Pharmacy at the University of Bradford whilst working for Bradford Particle Design. She… Read more »

Peter Coombs

Peter has worked within the GDP environment for 18 years, initially as a GDP Inspector for the MHRA and, since 2011, as an Operations Manager and a Senior Inspector. In these roles he has developed a comprehensive understanding of the UK GDP sector and the application of the various regulatory requirements within it. Peter joined… Read more »

Claire Glenister

Claire has worked within the pharma sector for the last 24 years.  The first 15 years of her career were spent working in a variety of roles for a global manufacturer.  These roles included Quality Manager for both manufacturing and non-manufacturing areas of the business and, latterly, as the site compliance auditor which involved undertaking… Read more »

Aswin James

A passionate and motivated professional with expertise in Pharmaceutical Quality Systems, Business Development and Project Management.