Peter Doherty Email & Phone Number

Computer Validation: Preparation and Execution of Protocols for analytical instrumentation, monitoring systems, and document management systems. Preparation of supplementary documentation (Design Specifications, User Requirement Specifications, Functional Specifications, Validation Plans, Traceability Matrices, etc.)Analytical Method Validation: Preparation and Execution of Method Validation Protocols in accordance with ICH Q2 GuidelinesTraining: Conducted extensive courses including; Good Laboratory Practices, Analytical Method Validation, Computer Validation, Pharmaceutical / Biotechnology ManufacturingAuditing: GLP Audits, Distribution Centre Audits, API Facilities

Richmond Hill, Ont. site (formerly Novex Pharma / NuPharm Inc.)Stability Chemist: Performed HPLC & GC Assays, Dissolution Testing, Degradation Product Testing, Karl Fisher, Raw Material Testing, etc. Also maintained Reference Standard Inventory, HPLC/GC column inventory, wrote Standard Operating Procedures, and provided training.Validation Consultant: Validation of Laboroatory Instrumentation (ChemStore network), Process Piping interfaces, and Building Monitoring System

Analysis of Raw Materials and Finished Products.Sat on a number of committees focussing on improving production efficienciesInteracted with clients on product development.Execution of Technology Transfer Protocols