Senior Regulatory Affairs Officer @ (August 2016 - February 2020)
Freelance Regulatory Consultant @ (August 2015 - August 2016)
Freelance Regulatory Consultant @ (March 2014 - August 2015)
Regulatory Affairs Officer @ Bio Product Laboratories (September 2005 - January 2014)
Chidi Nwanguma Skills
Regulatory Filings
Regulatory Affairs
Regulatory Submissions
Pharmaceutical Industry
eCTD
Clinical Trials
Generic Programming
Pharmacovigilance
Regulatory Requirements
Sop
Change Control
CAPA
CMC
FDA
GMP
GxP
Biotechnology
Validation
Standard Operating Procedure (SOP)
Electronic Common Technical Document (eCTD)
U.S. Food and Drug Administration (FDA)
Corrective and Preventive Action (CAPA)
Goal Setting
Performance Management
Chidi Nwanguma Summary
Chidi Nwanguma, based in London, GB, is currently a Regulatory Affairs Project Manager at Bio Products Laboratory Limited. Chidi Nwanguma brings experience from previous roles at Bio Products Laboratory Limited, The Janssen Pharmaceutical Companies of Johnson & Johnson and Bio Product Laboratories. With a robust skill set that includes Regulatory Filings, Regulatory Affairs, Regulatory Submissions, Pharmaceutical Industry, eCTD and more. Chidi Nwanguma has 3 emails on RocketReach.
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