Clive Edwards champions product quality at GlycoSyn, from the purchase of raw materials through to release of final product.
He was appointed Quality Manager in 2009, and oversees a rigorous quality management system that ensures regulatory compliance for international markets and gives staff the tools needed to contribute to continuous quality improvement of GlycoSyn’s product.
Clive holds a Bachelor of Science from the Open University in the UK along with post graduate qualifications in Software Engineering. He is an NZQA qualified Lead Auditor and has more than 20 years experience in the pharmaceutical industry working in both the manufacturing and regulatory fields.
His experience includes 2 years as a Senior GMP Consultant and 4 years as an Auditor for Medsafe (NZ Ministry of Health) covering a wide range of New Zealand’s pharmaceutical and complementary medicines industry. Before moving to New Zealand Clive Worked in numerous roles at Eli Lilly’s dry products manufacturing site in Basingstoke (UK), including Computer Systems Validation, Automation Systems Project Leader and Instrumentation Manager.