Pharmaceutical scientists involved with APS

Who We Are

The Academy of Pharmaceutical Sciences (APS) is the UK-based professional membership body for Pharmaceutical Scientists.

We represent individuals and organisations from around the globe, throughout their development, in the delivery of excellence in the Pharmaceutical Science sector.

Pharmaceutical Scientists are experts in the research, development and manufacture of medicines. They have a major role in the regulation of medicines and understanding their use in patients.

What We Do

The APS is a not-for-profit organisation. We use revenues to champion innovation and opportunity in Pharmaceutical Sciences thereby improving the development and delivery of medicines for the benefit of patients. Our four key strategic themes, which are the foundation of all APS activities, are:

  • Establish and promote the reputation of Pharmaceutical Sciences and Scientists
  • Influence policy
  • Further scientific knowledge
  • Promote careers

APS Priorities for 2022

  • Ensure that we continue to deliver high quality scientific content to our members
  • Attract and retain and diverse and engaged membership community
  • Deliver a successful face to face PharmSci conference in Belfast in September
  • Provide a vibrant Focus Group community with new groups aligned with current scientific areas
  • Promote and enhance diversity across our membership, board and fellows
  • Support and grow our accredited institution community

The APS Board

Dr Hannah Batchelor
Dr Hannah BatchelorChair
Dr Hannah Batchelor Is a senior Lecturer in Pharmaceutics, Formulation and Drug Delivery at the University of Birmingham.
Hannah is a pharmaceutical scientist who has worked in academia, the NHS and within pharmaceutical industry. Her research interests lie in the optimisation of drug formulations to maximise their biopharmaceutical performance and acceptability to children. Her research is informed by the views of children, young people and parents to ensure that the patients are at the centre of new developments.
She has been invited to present at many National and International scientific meetings as well as a TED talk.

Dr Begoña Delgado-Charro
Dr Begoña Delgado-CharroReader (Associate Professor)
M.B. Delgado Charro graduated in Pharmacy, received a PhD in Pharmaceutical Technology, and was a MEC-Fulbright fellow & visiting Assistant Professor at UCSF (1991-1993). She has worked as an academic at the Universities of Santiago de Compostela and Geneva, and since 2004, at the University of Bath where she is currently a Reader. She was a National Expert on Secondment at the European Medicines Agency (10/2015-9/2016) where she worked in business intelligence in drug development and Road-to-Market analysis.
Dr Delgado-Charro research focuses on transdermal and topical drug delivery, the development of optimized methods to treat and prevent nail diseases, non-invasive sampling for drug monitoring and pharmacokinetics, and the assessment of topical bioavailability and bioequivalence. Her work has been funded by several private and public sponsors and her scholastic work (Scopus author ID: 7003434711) includes 105 peer-reviewed scientific articles, 10 book chapters, and several patent applications. Her academic work focuses on the areas of pharmacokinetics and pharmaceutics in the frame of Pharmacy and Pharmacology degrees.
Dr Bahijja Raimi-Abraham
Dr Bahijja Raimi-AbrahamLecturer in Pharmaceutics
Dr Bahijja Raimi-Abraham is a pharmacist, Lecturer in Pharmaceutics at King’s College London and Founder of King’s College London Fight the Fakes and Academic Lead. She leads her research group “The Raimi-Abraham Group”. Her research to date has been in pharmaceutical materials and innovative manufacture. More recently she has focused her research efforts within the therapeutic and drug development aspects of malaria.

Prior to her current position as Lecturer in Pharmaceutics at King’s College London, Dr. Raimi-Abraham held positions at University College London (UCL) as an Engineering and Physical Sciences Research Council (EPSRC) postdoctoral researcher position and at the European Medicines Agency (EMA) as a seconded Quality National Expert.

Dr. Raimi-Abraham is the first graduate of the University of East Anglia School of Pharmacy to be awarded a Ph.D. and more recently won the Outstanding Woman in STEM Precious Award.

Dr Raimi-Abraham has an extensive and original public engagement portfolio which includes uniquely exploring the use of street art to engage public with Science, Technology, Engineering and Mathematics (STEM) research through her social enterprise STEAM:ED Collective, a TEDx talk (TEDx Talk title “Elements of Change: Becoming an Independent Researcher) and a “Go and No-go pills” Somerset House 24/7 exhibition, visited by ~35,000 people (Oct. 2019 – Feb. 2020)). More recently hosting a weekly podcast, Monday Science which discusses the latest in Science, Health and Technology. Dr Raimi-Abraham’s work in research informed teaching has also been recognised by the Nuffield Foundation.

Bob Clay
Bob ClayTreasurer
Bob Clay established his regulatory consultancy practice through Highbury Regulatory Science in 2014 which supports small/medium size companies and their investors to develop regulatory/business strategies across multiple therapeutic and geographic areas. Before this, he was a VP of Global Regulatory Affairs at AstraZeneca with responsibility for oncology, infection, and personalised healthcare. He is a member of the Expert Scientific Advisory Committee for Medicines for Malaria Venture (MMV) and works with several, not for profit organisations involved in global health initiatives. He was a board member of TOPRA (The Organisation of Professional Regulatory Affairs) from 2014 – 2018, and President for 2017.
Bob is a pharmacist with more than 30 years’ experience in drug development, leading the global regulatory approval of many products across a range of therapy areas including metabolic diseases, neuroscience, cancer, and infection, involving more than 15 new substances. Earlier in his career, he was a formulation scientist and pharmaceutical reviewer at UK regulatory agency. Bob has held significant leadership roles in regulatory affairs in regional and global functions at several companies including AstraZeneca and Pfizer and served as Chief Regulatory Officer at Kinapse (2014-2017).
Dr Julie Cahill
Dr Julie CahillProduct Development
Julie is Director, Product Development at AstraZeneca R&D.
Dr Kofi Asare-Addo
Dr Kofi Asare-AddoSenior Lecturer in Pharmaceutics, Admissions Tutor for Pharmacy (MPharm) Course at the University of Huddersfield
Dr Kofi Asare-Addo is a Senior Lecturer in Pharmaceutics and the Admissions Tutor for the Pharmacy (MPharm) course at the University of Huddersfield. Kofi became a Fellow of the Higher Education Academy in 2014. His research area includes UV imaging in pharmaceuticals, particle engineering, drug-clay complexations for oral controlled release formulation applications and solubility enhancements (solid dispersions, salts and cocrystals). His work has been presented both nationally and internationally at various pharmaceutical science conferences. Kofi successfully collaborates with other universities and several pharmaceutical industries.
Dr Philipp Seib
Dr Philipp SeibRegistered pharmacist and a Reader in Pharmaceutical Materials at the Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow
He obtained his BPharm and MSc from King’s College London and his PhD (2005) in drug delivery from Cardiff University. He conducted postdoctoral research at the Technical University Dresden (Germany) and Tufts University (Boston, USA). He is a Fellow of the Academy of Pharmaceutical Sciences and a Fellow of the Higher Education Academy. His research interest lies at the interface of cell biology, drug delivery and material science. His research mission involves top-down, challenge-based activities centred on developing pharmaceutical materials for healthcare technologies, with the ultimate goal of improving patient outcomes.
Jo Craig
Jo Craig
Jo is a Pharmacist and has spent her entire career working in the pharmaceutical industry with a focus on pharmaceutical development, product quality and the introduction of new manufacturing technologies. She is currently Senior Vice President CMC (Chemistry Manufacturing & Controls) for NeRRe Therapeutics, a clinical stage biotech company located at the Stevenage Biosciences Catalyst. She also held the same role for KaNDy Therapeutics prior to its acquisition by Bayer in 2020. Previously, Jo spent over 30 years at GlaxoSmithKline where her career spanned many leadership roles in CMC product development, most recently as Vice President of Technology & Strategy, Product Development & Supply. Jo led the technology team at the Medicines Manufacturing Industry Partnership (MMIP) 2017-2018 where she was influential in aligning Pharma and UK Government on future areas for investment as part of the Life Sciences Industrial Strategy. She continues to be involved with medicines manufacturing in the UK contributing to advisory groups. Jo is a Fellow of the Royal Pharmaceutical Society, an Eminent Fellow of the Academy of Pharmaceutical Sciences, UK and has been an Advisor to the APS Board for several years.
Professor Ryan Donnelly
Professor Ryan Donnelly Chair in Pharmaceutical Technology
Professor Ryan Donnelly holds the Chair in Pharmaceutical Technology at Queen’s University Belfast and is Director of QUB’s interdisciplinary research programme Materials & Advanced Technologies for Healthcare (MATCH). His personal research is centred on design and physicochemical characterisation of advanced polymeric drug delivery systems for transdermal and intradermal drug delivery, with a strong emphasis on improving patient outcomes. He is currently developing a range of novel microneedle technologies through independent research, but also in collaboration with several major pharma partners. He has obtained substantial UK Research Council, charity and industrial funding and authored over 300 peer-reviewed publications (H-index = 58), including 6 patent applications, 6 textbooks, 23 book chapters and approximately 250 full papers. He has been an invited speaker at numerous national and international conferences. Professor Donnelly is Europe/Africa Editor of Drug Delivery & Translational Research and the Controlled Release Society’s Communications Chair. He has won the Academy of Pharmaceutical Science’s Innovative Science Award (2020), Evonik’s Resomer Award (2018), the Controlled Release Society’s Young Investigator Award (2016), BBSRC Innovator of the Year and the American Association of Pharmaceutical Scientists Pharmaceutical Research Meritorious Manuscript Award (2013), the GSK Emerging Scientist Award (2012) and the Royal Pharmaceutical Society’s Science Award (2011).

The Advisory Board

Dr Linda Hakes
Dr Linda Hakes
Linda has more than 40 years’ experience in the pharmaceutical industry, having worked for companies such as Glaxo, Marion Merrell Dow, Celltech, Eli Lilly, Schwarz Pharma AG and UCB Biosciences. Her experience covers pharmaceutical development, preclinical development, clinical trial supplies, quality assurance and project leadership. Since 2016 Linda has been an independent consultant with a focus on pharmaceutical development and development strategy.
Linda is a Vice President of FIP (International Pharmaceutical Federation), a member of the Assembly of Royal Pharmaceutical Society (RPS) and the immediate past Chairman of the Academy of Pharmaceutical Sciences. She is also visiting Professor at Sunderland University and is eligible to be a Qualified Person. Linda is a Fellow of both the Royal Pharmaceutical Society and FIP.
Professor Trevor Jones
Professor Trevor Jones
Trevor is a Board member of the life sciences investment company Arix Bioscience plc; and the Oxford based Drug Discovery Company, e-Therapeutics. He was a Director of Allergan Inc. (USA), R&D Director of The Wellcome Foundation and Director General of The ABPI.
He holds honorary degrees and Gold Medals from 7 universities; is a founder member of Medicines for Malaria Venture (MMV); member of The UK Government Regulatory Agency, The Medicines Commission; advisor to the Cabinet Office on the Human Genome project; Chair of the UK Government Advisory Group on Genetics Research; member of the Wales Government Bevan Commission on health; advised the Government of the Netherlands TiPharma on Life Science and is a member of the EU Commission IMI Scientific Advisory Board.
Professor Mike Hannay
Professor Mike Hannay
Mike is Managing Director of the East Midlands Academic Health Science Network (AHSN), an NHS organisation charged with transforming the health of 4.6 million people living in the East Midlands and stimulating wealth creation in the region. Mike joined the NHS after 28 years developing new medicines. Mike has managed and contributed to the development of the formulations, devices, drug substance manufacturing processes and associated test methods for a number of innovative new medicines.
As a member of the Advisory Board Mike supports the board in developing strategies that promote the pharmaceutical sciences and encourage high standards of practice.
Professor Bill Dawson
Professor Bill Dawson
Bill Dawson is a previous Chair of APS and is now an Advisory Board member with responsibility for the accreditation process. His career was primarily in industry, mostly as Research Director for Eli Lilly and Co in the UK but has been an academic and a community pharmacist. Currently he runs a health care consultancy advising universities and SMEs on development and commercialisation of new medicines and devices. He is a visiting professor at the universities of Durham and Nottingham and is an external adviser to Stevenage Bioscience Catalyst, an open innovation campus.
Professor David Jones
Professor David Jones
Currently I am Pro-Vice-Chancellor (Education and Students) and Professor of Biomaterials Science at Queen’s University Belfast. As an internationally renowned pharmaceutical/biomedical engineer my research seeks to provide engineering solutions to medical and pharmaceutical problems. These include innovations in the design of drug containing implants and medical devices to that reduce the morbidity and mortality associated with medical device related infection. Commercialisation of this research has occurred and is ongoing. Within the pharmaceutical domain, I have developed novel implants for the treatment of local diseases and, additionally, engineering technologies to develop new dosage forms, including strategies in which drugs of low solubility (negating their clinical utility) may be developed for clinical usage.
Dr John Wahlich
Dr John Wahlich
John Wahlich is a chemist with over 40 years’ experience in Pharmaceutical Development gained with a number of major pharmaceutical companies. He obtained his BSc from Bristol University and his PhD (part-time) from University of Nottingham School of Pharmacy. Until November 2010 he was a Vice President in GlaxoSmithKline and ran various multi-national departments involved with analytical chemistry, Product Line Extension development, physical properties and developability and early stage CMC support. He has a good knowledge of Quality by Design, Change Control and Technology Transfer. He is currently CEO of John Wahlich Associates Ltd a consulting company specialising in the pharmaceutical sciences. John is currently consulting for a number of companies on early stage product development. He is an Advisory Board member of the UK Academy of Pharmaceutical Sciences (APS), has co-hosted successful workshops on drug developability and has co-organised a number of APS International Pharm Sci conferences (the UK’s premier Pharm Sci event).

Dr Tommy Dolan
Dr Tommy Dolan
Tommy completed his undergraduate and postgraduate education in Pharmacy at the University of Strathclyde. Following that he undertook post doctoral study at the universities of Strathclyde and Glasgow assessing novel drug carrier systems as immunological adjuvants. He first joined Controlled Therapeutics in 1988 where he was involved in researching the use of hydrogels as novel drug delivery systems for a range of indications. In 1990 Tommy commenced his career at Pfizer Global Research and Development at Sandwich joining as a formulation scientist. Since joining Pfizer he has held a variety of positions in Pharmaceutical Research and Development in that time ultimately heading the department since 2002. Tommy has been involved in the development of a number of drug development programs and wide variety dosage form types in that time many of which are now marketed products.
Dr. Kendal Pitt
Dr. Kendal PittSenior Technical Director
Dr. Kendal Pitt is a Senior Technical Director based at GlaxoSmithKline(GSK) in the UK and works in the Manufacturing, Science and Technology (MSAT) group. He is a Fellow of the Royal Pharmaceutical Society (FRPharmS), an Eminent Fellow of the Academy of Pharmaceutical Sciences and an Honorary Professor at Leicester School of Pharmacy, De Montfort University. He has worked in the Pharmaceutical Industry for over 30 years in both R&D and Production. Kendal has headed groups in both the United States and Great Britain and led project teams responsible for the successful filing and launch of tablets, capsules, and freeze-dried dosage forms.