David Waddington’s career in the pharmaceutical industry spans more than 30 years in various quality roles for three major international pharmaceutical organizations. His most recent appointment was Quality Director, Global Regulatory Compliance for Catalent Pharma Solutions. He joined NSF in July 2017.
Mr. Waddington is eligible to be nominated to act as a Qualified Person under the permanent provisions. He has broad experience in QA and manufacturing management gained through working with a wide range of dosage forms for global supply including solids, liquids, sterile products, food supplements and natural products.
Mr. Waddington is fully conversant with current EU and FDA GMP regulations and requirements. He has extensive experience in international QA auditing of a wide range of pharmaceutical suppliers and manufacturers in Europe, North America and Asia-Pacific.
His recognized expertise includes:
- GMP legislation
- Regulatory compliance
- QP training
- Packaging and labeling control
- Analytical testing
- Auditing and self-inspection