Mark Read Email & Phone Number

Dereham, Norfolk England

Drafting, generation and issue of technical manuals, user guides, training material, spare parts guides, quick guides, product instructions and datasheets via hands on product use and installation; using Adobe CC InDesign. Generation of Interactive pdf's with Adobe acrobat DC.3D product part and assembly modelling, & drawing creation using Solidworks.3D motion studies, rotates, explodes etc. using Solidworks.2D drawing using Draftsight.Creation and manipulation of raster images and vector graphics using Adobe CC – Illustrator and Photoshop.Creation of training videos via 3D motion studies exported from Solidworks, using Adobe Premier Pro & Media Encoder.Mapping interlinked business processes using MS Visio.Generation of formal written business processes, SOPs, Instructions, templates & other standard QMS documentation in MS formats.Document publishing for print and web media.

Gt Yarmouth, Norfolk, England

Team leader for high temperature thick film hybrids and multichip modules electronics development programme, for the oil and gas and aerospace markets.Review of customer product specifications, leading the development phase through to manufacture for product ranging from complete radar through electronic modules to PCBAs, and thick Film ceramic substrates and hybrids. Understanding & working to electronics manufacturing standards inc. IPC-A-610, IPC-A-600 etc. Manipulation of customer CAD data. Meeting, liaison and ongoing support for customers, to discuss the product in terms of technical requirements, quality and build standards.Generating AutoCAD piece part & assembly drawings, graphics & Gerber design data.Working to AS9100 Aerospace & ISO13485 medical, quality standards.Creation & control of BOM, method route & manufacturing data pack.

North Walsham, Norfolk, England

Product development and support from design stage through production to final release and customer support; for a range of products in the food, packaging and agricultural industries. These include air cushion packaging machines, bulk grain samplers and in process pellet testing & analysis equipment.Generating AutoCAD drawings of machine parts, components, site plans etc. Supporting manufacturing in the generation of BOMs on ERP system, generating work instructions and route sheets.Supporting customers with telephone and email product technical advice and fault finding. Supporting the Managing Director in research, development and implementation of quality and regulatory processes and procedures related to EC new approach directives, CE marking and the ISO9001:2000 quality management system. RoHS & WEEE.Supporting international sales engineers with system specifications site requirement and site plans.

Quality Assurance Manager, (contract) Arena ZME Ltd. QMS Update to ISO9001, ISO13485 and FDA QSR (CFR820) compliance.Rewriting the quality and procedure manuals.Regulatory advice and assistance to customers for FDA 510k and CE MDD approvals for all classes of device.Undertaking ISO14971 qualitative medical device risk management.Leading customer and notified body audits, internal auditing, complaint handling and CAPA.Institution of systems for continual process improvement, institution of customer satisfaction processes and their analysis.Institution of a system of network based hyperlinked flow diagrams, to demonstrate the process approach of the QMS, and to reduce paper copies of procedure, work instruction and work record manuals.Anglia Vale Medical. Contract to update the quality system to ISO13485, ISO9001Harnser Systems Ltd. Contract to manage CE marking for cranes.Bulbrook Associates. Contract to manage CE marking for medical and electro-medical devices.

Norfolk England

Overall responsibility for the production and testing of Nerve Stimulators and probesProject management of new devices.• Institution and maintenance of an ISO9001, ISO13485 (for medical devices) and FDA CFR820 compliant quality system.CE marking for MDD (Medical Devices Directive 93/42/EEC), Class 2a & Class 1 equipment.FDA 510k approvals for class 11 equipment.EU Authorized representation for non-EU manufacturers.ISO14971 Medical device risk management.Medical devices regulatory assistance for non-EU and US approvals.Monitoring BS EN and ISO Standards, to ensure production and OEM equipment conform to the required standards and therefore meet the essential requirements of the MDD & relevant FDA CFRs.Production cost savings, around 10% of turnover.Production and customer returns, faultfinding and analysis.

Lowestoft, Suffolk, England

Development and manufacture of one off or small batch electronic equipment for and including: Automatic and manual test facilities and burn in & endurance facilities for a wide range of products in the aerospace industry. Electronic equipment for underwater cameras, pipe crawlers, wildlife tracking systems, wrapping machines, cutting machines.Component level faultfinding and repair of existing equipment.

Norwich, Norfolk, England

Component level fault finding of AV equipment for large scale manufacturersDevelopment and manufacture of test panels

Autodesk Autocad Essentials

Hnd In Electrical And Electronic Engineering, Electrical And Electronics Engineering, 2 Distinctions

Ond In Technology (Engineering)