Head of Quality
Daniel has over 15 years of experience in manufacturing, quality assurance, quality control, validation and product development in the pharmaceutical and biotech industries. This includes successful leadership, development and implementation of quality management systems, training and compliance programs and process improvement.
Daniel has held various quality assurance, compliance, microbiology and project management roles at CSL Seqirus, CSL Behring and Catalent Pharma Solutions. He brings knowledge and experience in the areas of pharmaceutical manufacture (API & FDF), quality assurance, validation and GMP compliance. He has worked at different stages of commercial drug manufacture for solid dosage forms (tablets and capsules) and sterile injectables (solution and lyophilised), and has contributed to the development, technology transfer and registration of pharmaceutical products.