With over 20 years of experience in Quality Management, Regulatory Affairs, Research and Development, within the analytical chemistry, pharmaceutical (solid dose, liquid dose, inhalers, oral-mucosal and radiopharmaceutical), and medical device industries. I am a subject matter expert in pharmaceutical stability, where my analytical skills and regulatory knowledge are used to ensure product quality and patient safety. My experience spans the entire product lifecycle, from initial research through to market launch and post market surveillance.In addition to my technical expertise, I am a seasoned leader adept at managing interdisciplinary teams and contractors to deliver high-quality R&D projects on time and within budget. I have knowledge and experience in regulatory adherence to GLP, GMP, ISO, and ICH standards across a variety of regulatory bodies, including TGA, MHRA, ANVISA, and FDA.