Peter Jordan

Peter Jordan has over 20 years experience in the pharmaceutical industry. He started in bench process development chimeric protein therapeutics and has experience in sterile manufacturing and fill (E. coli, yeast, and CHO/NSO expressed products) including mAbs, ADCs, bispecifics, and development of gene and cell therapies. Peter has experience in virus clearance management and scale down study technology transfer and GLP study execution along with Person in Plant representation for multiple products (biologics and small molecules). Other areas of speciality are Quality assurance for clinical and marketed products (sterile/non-sterile) including Lead Auditor supporting routing, ‘for cause’, and remediation of Agency findings and Regulatory affairs CMC writer / reviewer.