Anthony Williams

WORK HISTORY

EDUCATION

SKILLS

ABOUT ANTHONY WILLIAMS

Profile:Electrical Engineer with 40 years’ experience of installation, commissioning, servicing and validation of Pharmaceutical, Cosmetic, Bio-Pharm and Medical Devices equipment including high speed blister packaging lines, High speed bottle tablet lines, OSD pharmaceutical manufacturing facilities, utilities and equipment on a global scale, Supported by 10 years’ experience in management of capital investment projects.Key Skills and Aptitude:GMP Engineering background. Excellent Communication and Interpersonal Skills. Has a passion for Engineering Excellence. Able to negotiate and present own ideas to a wide audience. Adaptable and Flexible to cope with the changing needs of the production environment. Ability to identify opportunities for process and operational improvements and implement appropriate changes to deliver these benefits. Passion for “right-first-time” processes and a determination to understand breakdown or failure to root cause and prevent re occurrence. Ability to prioritise and plan own work. Highly competent in all aspects of Engineering including Electrical, Electronic, Pneumatic, Hydraulic, Mechanical and Instrumentation.Key Achievements: Writing and Execution of validation protocols for New Oral Solid Dose Pharmaceutical Manufacturing Facility including Building Fabric, Clean Rooms, Classified Areas, Non-Classified Areas and Warehouse. HVAC Systems - Air Flows, Air Changes, Pressure Cascades, Temperature Control, Humidity Control and Temperature Mapping, EMS System - Digital Recorders, BMS System, Utilities – Purified Water, Softened Water, Compressed Air, Blender – Muller, Quadro Comil, Tablet Coater – Manesty, Compression Machines – Fette, hoists, IBC’s, IBC Washer, Granulator – Glatt, High Shear Mixer – GEA, Fluid Bed Dryer – GEA, Sieve and Dispensary – Russell Finex, Clean in Place Systems.Planning and execution of Engineering Projects, Preparation and Execution of life cycle validation documents including VMP, PVP, VP, URS, FDS, SDS, HDS, DQ, EQ, IQ, OQ, SOQ, PQ, PV, ERES, GAMP, CSV, Cleaning Validation, SIP, CIP Systems. Installation, Commissioning & Validation of high speed Blister packaging lines, High Speed Tablet Bottle lines, Bio-Pharm and Medical Devices equipment. Management of Engineering Teams and budgets. Change Control, Deviation Management, CAPA, Root Cause Analysis, SPC & Continuous Improvement Projects. Preparation of facility, equipment and documentation for FDA and MHRA audits. Highly conversant with the FDA, MHRA, ISPE, CGMP, 21 CFR Part 820, 21 CFR Part 11, ISO 13845 regulations and guidelines.