Francois Vandeweyer, PE
Janssen Pharmaceutica
Director Pharmaceutical Regulatory Compliance EMA
Francois Vandeweyer joined Janssen Pharmaceutica (part of Johnson & Johnson) in 1981 in chemical
development. Until 1995 Francois had increasing responsibilities within the organization mainly in the
Quality Control Unit. Starting from 1995 he joined the QA department and headed several Senior Manager responsibilities. In 2005 Francois was promoted to Senior Manager GMP Compliance Chemical Operations Belgium
(sites Geel – Olen – Beerse). In 2009 Francois joined the Enterprise Regulatory compliance group of J&J in the function of Director Pharmaceutical Regulatory Compliance EMEA.
Francois is member of APIC since 2005, currently he is Vice Chair of the APIC Quality Working group and heading 2 task forces. 3rd Party Auditing and ICH Q7 “How to Do”
development. Until 1995 Francois had increasing responsibilities within the organization mainly in the
Quality Control Unit. Starting from 1995 he joined the QA department and headed several Senior Manager responsibilities. In 2005 Francois was promoted to Senior Manager GMP Compliance Chemical Operations Belgium
(sites Geel – Olen – Beerse). In 2009 Francois joined the Enterprise Regulatory compliance group of J&J in the function of Director Pharmaceutical Regulatory Compliance EMEA.
Francois is member of APIC since 2005, currently he is Vice Chair of the APIC Quality Working group and heading 2 task forces. 3rd Party Auditing and ICH Q7 “How to Do”