Sanjay Nadarajah has dedicated his career to raising the standards of pharmaceutical quality on a global scale. He holds a bachelor’s degree in Chemistry and is a Fellow of the Royal Society of Chemistry, in recognition of his outstanding services to the pharmaceutical industry.
With experience spanning startups to multinational pharmaceutical companies, Sanjay specialises in implementing and optimising quality processes and building genuine quality cultures within organisations. He believes that quality should not be the preserve of large, well-resourced businesses, but should be accessible to all.
That belief has shaped his work as an entrepreneur and philanthropist. He has founded several startup businesses and is a committed champion of the next generation of pharmaceutical quality professionals, supporting individuals to grow and progress in their careers. He founded the largest LinkedIn group dedicated to freely sharing knowledge on Good Manufacturing Practice and Good Distribution Practice, a community built on the principle that open access to quality insight benefits the entire industry.
Outside of work, Sanjay enjoys spending time with his family and taking long walks with his two German Shepherds.
Anju Nadarajah brings a distinctive perspective to pharmaceutical quality, one rooted in finance. A graduate of University College London with a degree in Economics, she is a Fellow Chartered Accountant with the ICAEW.
Her path into the pharmaceutical world began through reviewing quality-led GxP site audit reports, where she immediately recognised the connection between financial discipline and pharmaceutical quality management. She saw no reason why the two should be treated as opposing forces and set about proving they do not have to be. Why should finance and product quality conflict, when synchronising them could enhance global access to medicine?
That philosophy drives everything Anju does at Inglasia Pharma Solutions, where she has pioneered initiatives that make quality more accessible and affordable for companies of all sizes, without compromising on the highest standards of pharmaceutical quality management systems.
Outside of work, Anju is training as a Bharata Natyam South Indian classical dance performer, sings, and loves playing the violin. She is also a devoted fan of elephants.
Lynne Butcher is the EU Qualified Person at Inglasia Pharma Solutions Ireland, bringing over four decades of experience to the role, though as she will tell you, she was very young when she started out.
She holds a BSc Hons in Chemistry from Kingston University and a Postgraduate Diploma in Industrial Pharmaceutical Studies from the University of Brighton, passed with Distinction. Having qualified as a QP under the UK process prior to Brexit, she holds the increasingly rare distinction of being eligible to act as both a UK and EU Qualified Person, a credential she has held for 23 years.
Her career spans an exceptional range of pharmaceutical environments, from large-scale oral solid dose manufacturing and parallel import operations handling over a thousand products, to immunology and named patient products, giving her a breadth of regulatory and quality expertise that is genuinely difficult to match. A Lean Six Sigma Green Belt, experienced investigator, auditor, and author of technical reports across the full spectrum of regulatory variations, she has provided quality leadership under both IAG and CMT oversight, with particular depth in Annex 1 compliance, contamination control strategy, and CAPA remediation.
Highly analytical by nature, Lynne has an exceptional ability to absorb and process large volumes of complex data, translating it into clear, quality-focused decisions with confidence and precision. What sets her apart further is her ability to hold the line on quality and patient safety without losing sight of the commercial and operational pressures that businesses face. She understands that in the real world, integrity and pragmatism must work hand in hand.
That commitment to the profession runs deep. Lynne serves voluntarily across several forums within the Royal Society of Chemistry, shaping the standards and conduct of the profession and ensuring those who follow in her footsteps are held to the same exacting standards she has always set for herself.
Outside of work she enjoys reading, knitting, jigsaws, gardening, and is currently studying for her GCSE in Spanish. She has also, on one notable occasion, been sawn in half by a magician.
Zara Khan is a Quality Assurance Manager and Responsible Person with deep experience in pharmaceutical quality systems, wholesale distribution compliance, and the oversight of imported medicinal products within UK and EU regulatory frameworks.
As a UK Responsible Person, Zara ensures wholesale distribution activities operate in full compliance with GDP requirements, overseeing that medicinal products are stored, handled, and supplied in line with MHRA and HPRA expectations. Her work spans both GMP and GDP environments, encompassing deviation and CAPA management, supplier qualification, technical agreement oversight, and batch documentation review, supporting organisations in building and maintaining strong, inspection-ready compliance frameworks. She works closely with Qualified Persons, regulatory specialists, and supply chain partners to ensure products consistently meet regulatory standards before reaching patients and markets.
Zara approaches quality with what she calls a “chess mindset”, mapping out every possible scenario before recommending a course of action. It is an approach underpinned by a deep, hands-on understanding of regulatory requirements, from setting up manufacturing machinery and laboratory equipment to representing clients through regulatory inspections and new customer audits. Known for remaining calm and collected under pressure, Zara is a steady and trusted presence in complex troubleshooting situations, the kind of person you want in your corner when the stakes are high.
Outside of work, Zara is a keen traveller with a passion for gym training, fashion, and makeup. She is also a self-confessed car enthusiast, equally at home discussing performance specs as she is the latest runway trends.
Dariia Matskiv is a QA Associate at Inglasia Pharma Solutions Ireland, Dublin based with a permanent presence at the main office. She is completing her bachelor’s degree in Chemical Engineering, building a strong scientific and technical foundation that enriches her work in pharmaceutical quality.
Her academic background is further underpinned by an exceptional aptitude for science, demonstrated by her achievement of a national award in the Biology Olympiad of Ukraine.
In her role, Dariia supports the Quality team in maintaining and upholding quality standards, contributing to key Quality Management Systems and compliance activities under the Manufacturing and Importation Authorisation. She brings a strong focus on continuous improvement and teamwork and takes genuine satisfaction in supporting colleagues across day to day quality operations.
What makes her particularly distinctive is her rare ability to take complex technical and regulatory concepts and communicate them in ways that are clear, engaging and genuinely accessible, a skill she has actively cultivated, having founded an academic support group to help fellow students build confidence and performance in mathematics, biology, and chemistry.
A natural collaborator and creative thinker, Dariia approaches every challenge with both analytical precision and imagination. Outside of work, her interests are as eclectic as her skillset, spanning hairdressing, drawing, sculpture, sewing, and volleyball.
Dr Ghada Amami holds a National Doctor of Pharmacy Diploma from the Faculty of Pharmacy of Monastir, one of the most prestigious pharmacy institutions in North Africa, and brings to her role as Senior Quality Assurance Associate at Inglasia Pharma Solutions a depth of expertise spanning clinical practice and pharmaceutical quality systems.
Her early career placed her at the sharpest end of patient safety, serving as the appointed pharmacist for an infectious diseases department, where she reviewed high-risk prescriptions for some of the most vulnerable patients, those living with HIV/AIDS and those in intensive care. Managing complex polypharmacy, where unchecked drug interactions can be fatal, demanded both rigorous clinical precision and genuine compassion. She also conducted patient exit interviews, ensuring individuals leaving care understood their treatment and could manage it safely. It is a background that gives her an understanding of patient safety that goes far beyond regulatory theory. She has seen first hand what is at stake.
That clinical foundation now informs her specialism in GDP and GMP compliance and Computerised System Validation, where she is a certified specialist in CSA and GAMP 5 principles. Ghada is responsible for the strategic oversight of the MIA Quality Management System, providing expert guidance on GxP governance and building lean, inspection-ready quality systems that are robust without being over-engineered.
She has a particular talent for identifying gaps, assessing what exists, recognising what is missing, and reworking procedures to be sharper and fully compliant. Every project she takes on is approached as though it were her own creation, driven by genuine passion and an unwavering sense of personal accountability. Nothing is left unfinished, and nothing leaves her hands until it meets the standard she has set for herself.
Her research on pharmaceutical waste management was awarded Highest Honors, a fitting recognition for someone who brings that same level of dedication to everything she does.
Outside of work, Ghada is a passionate ambassador for Tunisian culture and cuisine, and enjoys spending time with family and friends, travelling, and exploring the outdoors, always in search of the best local coffee. She is also on an ambitious culinary journey, striving to one day match the cooking of her mother, which by all accounts sets a formidably high bar.
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