Tess is a distinguished Quality Professional with 20 years’ experience in the Pharmaceutical and Medical Device Industries.
Tess Egan has been involved in formalizing, operating within & auditing Quality Systems and Facilities for compliance with a wide array of global regulations across the Globe including GMP, GLP, GCP, GcLP, GDP, ISO 13485, ISO 9001, and ISO/IEC 17025.
During her distinguished career, she has been involved in Manufacturing, Contract Research, Affiliate Support, and Vendor Approval and Management.
Tess is a former Regional Compliance Auditor for Abbott Rapid Diagnostics Division responsible for the planning and execution of independent Regional Compliance audits for Divisional regulated entities in the EMEA region. In addition, she performed audits in the APAC & Americas as well as third party supplier audits globally.
Within her previous roles in both the pharmaceutical and medical device sectors, she has formalized various training programs, including Auditor training, for the companies she has worked with & we are delighted to welcome Tess to the Comply Guru family!