Pharmaceutical Course Tutors
John Dolman
John has held senior Quality roles in several of the major companies and is a former chairman of the Royal Society of Chemistry's panel of Qualified Person (QP) assessors. He has wide experience of the development, manufacturing, quality control and regulatory aspects of many dosage forms gained from spending over 30 years in the Pharmaceutical Industry. John is now one of the key tutors on RSSL's QP Training Programme.
Aidan Madden
Aiden Madden (BSc, MSc, Qualified Person) is the new tutor for RSSL's popular Lead Auditor training course. Aidan has worked as a consultant with a number of pharmaceutical manufacturing companies in Ireland, Belgium, Netherlands, Italy, Spain, USA and Turkey. He has 4 years' experience in R&D and 12 years' experience working in Biopharmaceutical and Pharmaceutical Manufacturing with companies such as Fort Dodge Laboratories, Baxter Healthcare and Wyeth Medica Ireland.
Anthonia Chalmers
Anthonia is a qualified pharmacist with 30 years experience in the pharmaceutical industry, most recently as Head of Clinical QA of Celltech Medeva. Her experience embraces Research, Regulatory Affairs and Compliance. As well as being a member of the British Association of Research Quality Assurance and a founder member of its GMP Committee, Anthonia holds professional memberships of TOPRA and the Institute of Clinical Research. She is also a nominated QP on the Manufacturing Authorisation for Investigational Medicinal Products of a commercial Phase I unit.
Ashley McCraight
Ashley specialises in the auditing of suppliers to the Pharmaceutical Industry. He has over 25 years experience of working in Quality Assurance and Quality Control activities, primarily for GlaxoWellcome. He is a Qualified Person and recently worked as leader of the Pharmaceutical Quality Groups "Partners Team", who updated the "Pharmaceutical Suppliers Codes of Practice" for in line with the new ISO9000: 2000 standard.
Christopher Burgess
Christopher is Principal of Burgess Consultancy, an Independent Consultancy in Analytical Science specialising in the validation and qualification of computerised analytical instrument systems. He is a Qualified Person and has spent 20 years with Glaxo Operations in Quality Assurance and related activities. He is active within the Analytical Division of the Royal Society of Chemistry's Analytical Methods Committee and the Ultra Violet Spectrometry Group. His publications include editing and contributing to 5 books and over 40 papers.
Keith Dobson
Keith has held senior Quality roles in several of the major pharmaceutical companies and is a former QP assessor for the Royal Society of Chemistry. He has a wide experience of the development, manufacturing, quality assurance and regulatory aspects of both API's and dosage.
Rick Maddock
Rick has over 30 years experience in the pharmaceutical industry having worked in Quality and Production departments concerned with a wide range of dosage forms. He has considerable international experience having been involved in manufacturing and validation projects in many overseas territories. For the last 4 years Rick has been a practising consultant focussing on Quality Systems, auditing and validation activities.
John R Cooper
John began his career in the pharmaceutical industry in 1976 in analytical chemistry laboratories and moved on to manage various quality functions. During this time he was responsible for a wide range of activities including wet chemistry, intermediate and finished product testing and Vendor Audits. In 1989 John moved to Packaging Quality Assurance and was the main site QP for ten years. In 1999 he moved into New Product Introduction and was responsible for leading multi-disciplinary teams transferring a number of global products from R&D to packaging, and in 1999 this role was combined with an Artwork and Design group which John led for five years until December 2005. John now leads the Packaging Manufacturing Support organisation and is involved in Packaging transfers and new business introduction.
Brian Hammond
Brian has over 30 years of experience in the bulk pharmaceutical industry working for GlaxoSmithKline. He has extensive experience in many aspects of process and plant cleaning validation, analytical techniques, auditing & Good Manufacturing Practice.
Peter Willis
Peter is a Freelance Pharmaceutical Quality Consultant advising the pharmaceutical and biotechnology industries and their suppliers and contractors. He has over 20 years experience in the industry, including 10 years in consultancy, with the remainder spent in site and corporate quality assurance roles for SmithKline Beecham, Zeneca and GlaxoWellcome where he was responsible for the preparation for and management of regulatory authority inspections.
Robert Cook
Bob is a chemist with more than 20 years experience in pharmaceutical development and Quality Assurance, most recently responsible for Research and Development Quality Assurance at the Aventis Pharma UK sites. He was a founder member of the BARQA GMP committee and is now a pharmaceutical R&D consultant.
Trevor Coomber
Trevor is a Pharmaceutical Development Consultant with over thirty years experience in the industry. He spent six years as a Senior Project Team Leader and Analytical Science Manager in Pharmaceutical Development in Glaxo Wellcome. Prior to that he was a Team Leader in the Analytical Development Laboratories in Wellcome where he developed and validated analytical methods and served on project teams including leading the Technical Development (CMC) of Valtrex Tablets from the molecule to the market place.
Raymond Munden
Ray has worked in the pharmaceutical R&D industry for more than 32 years, his most recent position being Head of Analytical Services Europe for GlaxoSmithKline, responsible for the release of raw materials, comparator testing, degradation chemistry studies, cleaning verification and for stability facilities. He has an extensive knowledge of pharmaceutical development, with particular expertise in analytical method development and validation, analytical equipment qualification, stability requirements, degradation chemistry studies and chemometrics and is now a Pharmaceutical Development Consultant and a visiting Fellow at Nottingham Trent University.
Ciaran Brady
Ciaran Brady has 25 years experience in Supply Chain/Materials Management in the Pharmaceutical, Healthcare and Drinks industry. He is currently Managing Partner of PLS Pharma Logistics engaged in the provision of a range of tailor-made Purchasing, Logistics and Supply Chain Management Solutions for the Pharmaceutical& Allied Supply & Service Sectors. Services include, Consulting, Coaching, Education, Training and Responsible Person Services. Ciaran Brady has working for major multinational pharmaceutical companies at a senior level mainly in Supply Chain/Materials Management areas.
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