Louis Angelucci

Louis Angelucci is currently Senior Project Management consultant with Johnson and Johnson specializing in engineering initiatives regarding Qualification, Validation and Compliance. Mr. 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 and CQA and is currently the ASQ Philadelphia chapter Education Chair. In addition, he holds a PMP certification through the Project Management Institute.

Mr. Angelucci is a member of the IVT board of Directors and has been a contributing speaker to IVT since the organization’s early beginnings. He has published numerous articles on the subjects of Validation and compliance and has been a speaker to industry groups such as ISPE, IDE, PDA and ASQ.

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