UK qualified Pharmacist with over 20years experience leading, managing and supporting the development of pharmaceutical and biopharmaceutical (biosimilar) products in diverse, multi-cultural and multidisciplinary project teams within global organisations.
In-depth knowledge of quality systems, R&D processes, International regulations, EU GMP, GDP and GCP regulations, with a strong background in Quality Assurance, Vendor management, Clinical Trial Supplies manufacturing, packaging and distribution, regulatory inspection preparation and support across multiple dosage forms.