Louis Angelucci is a pharmaceutical professional with over 20 years experience in Quality Assurance, Quality Control, Regulatory Affairs, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries. He has worked for several well-known companies, including Johnson & Johnson, Bristol-Meyer Squibb, Pfizer, Schering Plough and Merck. His experience has been either as a direct employee or as a contracting consultant while employed at Foster Wheeler and Aker Kvaerner. As a consultant, Mr. Angelucci has worked at various project locations domestically and in Europe and Asia.
Mr. Angelucci is a degreed engineer with two master’s degrees in engineering, holds industry certifications with ASQ as a CQE, CQA and CPGP. He is currently the ASQ Philadelphia chapter Education Chair. In addition, he holds a PMP certification through the Project Management Institute. He has published numerous articles on the subjects of Validation and compliance and has been a speaker to industry groups such as ISPE, IVT, DIA, PDA and ASQ.
