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Principal Consultant 001

Principal Consultant brings clients more than 23 years of experience in quality management in both the Pharmaceutical and Medical Device development and manufacturing industries. He is an expert in Quality System development and reengineering, which makes him a valuable asset to the BEQS Engineering & Compliance Practice. His strengths includes Auditing, Equipment & Process Validation (IQ/OQ/PQ/R&R), Six Sigma, Training, and Software Development Lifecycle. Principal Consultant started as a Chemist and Group Leader in Drug Manufacturing (LVP, SVP and Combination Devices) responsible for in-process and finish product Chemical Control testing and later Quality Engineering for five drug manufacturing lines, including product complaint investigations. It was here that he received direct training from Dr. Deming in TQM. He later moved to Quality Engineering and Quality Management for several device firms, responsible for Quality System development, Software Quality assurance, Metrology, Supplier QA, and Six Sigma. Principal Consultant has spent the last 10 years consulting with and for ex-FDA District Directors, auditing and developing/remediating Quality Systems for both the Pharmaceutical & Medical Device Industry. He is most recognized as a Quality Systems & Quality Engineering expert, and for excellent training skills and the development of Strategic Regulatory Solutions.



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