Our UK Centre is run by Bob Page, Martin Shaw, and Niall MacLoughlin.

Bob runs his own consulting firm called Reliability Plus out of London, Martin runs his own consulting firm Reliability Solutions out of Scotland, and Niall runs his own consulting firm Pharos Quality Solutions out of Ireland.

Ops A La Carte has teamed up with reliability all three to form a UK alliance. Each company has a specialty in its own, and each is geographically positioned to service not only the UK, but all of Europe and beyond.

Bob's expertise is in training seminars, hands-on workshops and regular project management. Bob provides expert independent guidance and practical assistance to companies wishing to implement and/or enhance their HALT/HASS and stress screening capabilities. Hundreds of engineers from leading companies such as Eaton Aerospace, Filtronic, Renishaw, and Westinghouse have benefited from Bob's expertise, encompassing a broad range of engineering market sectors.

Martin's has consulted / worked extensively throughout Asia, USA and Europe. His role as specialist in product and commodity quality reliability optimisation gave him an in-depth understanding and insight of manufacturing process problems across a wide range of suppliers. Since establishing Reliability Solutions in 1997, Shaw has further broadened his knowledge and expertise in the field through working closely with companies within the Asia/Pacific rim region. From them, he has gained experience in dynamic work environments where rapid improvement is expected at all times. These companies include Daewoo, LiteOn Tech, Astec Power, Samsung, Philips, AOC, Vestel, Acer, Royal, LiteOn Power, Heng Sheng Optoelectronics, Amtran, Fairchild Semiconductor, etc

Niall specializes in Quality & Design Assurance Services to the Medical Device Sector. His specialties include: Internal Auditor Training Courses in ISO 13485, ISO 9000 & ISO 14001; Design Controls Training Course in compliance with ISO 13485 & FDA QSR; Internal Audits, Supplier Audits, Design System Reviews (Qualified Auditor); Software Validation in compliance with FDA CFR Part 11; Medical Device regulatory submissions FDA 510k and CE Mark; Quality Management Systems Development and Certification activities; and General Medical Device (Class I & II) consulting and mentoring activities.

We shall utilize this alliance the skills of all three of these talented consultants for projects in the Europe and Asia regions.

Email: via our contact form

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