Peter van 't Veld

Ready to make quality work for your organization | Pharma and Food industries | Highly experienced quality manager Interim Quality Management and dedicated QA support activities like: o Setup/optimize the quality management system o Harmonize different quality management systems (GMP-FSSC-ISO) o Audits of suppliers, service providers and contractors o Internal audits o Setup / improve supplier management o QA support in major projects (expertise ICT and DMS/QMS) o Training on quality aspects

Responsible for overall quality approach within the Corbion sites worldwide concerned with manufacturing of lactic acid and derivatives. Setting out quality directives for the quality framework covering and meeting feed, food, and pharma (API and excipients) regulations, and ISO9001/14001 requirements.

Responsible for all quality aspects on contract manufacturing in Europe and Asia and supplier management for ingredients in feed, food, pharma and technical applications. Setting up a qualification and risk based monitoring system on quality performance of Contract Manufacturers. Lead auditor in all contract manufacturer and supplier audits. Review and approval of quality agreements/contracts with Contract Manufacturers, suppliers and customers.

Designing and setting up a lean integrated ISO/GMP quality system for R&D in vaccines, leading to granting of manufacturing license. Responsible for all QA activities including supplier management and auditing of suppliers, guiding and hosting customer and regulatory inspections. Managing all quality related aspects in vaccine development projects with third parties.

merging and implementing GxP activities related to the Dutch vaccines program from former NVI (Dutch Vaccines Institute) into existing RIVM (Governmental institute on public health and environment) (ISO) quality system. Managing activities of QA department. Responsible for quality management of the Dutch vaccination program

QA manager for the QA team, performing the QA related activities in production and new projects for the manufacturing of vaccines. Responsible for the QA system including training and coaching of new employees and lead / quality responsible for in supplier management and auditing. QA activities in larger investment projects (e.g. new facilities). Coordinating the activities of the QA projects group. Addressing all GMP aspects in the development of polio and influenza vaccines for the WHO.

Pharmacotherapy, Quality of Care and Health Information, Research and Innovation, International Pharmaceutical studies.