Bertrand Gabry, Bill Muirhead and Charles Fontannaz worked extensively together for Valtronic Technologies.
The three friends and work colleagues had the ambition to use their complementary experience and skill-sets to create a global Business Consulting firm able to bring entreprising solutions adapted to the needs of regional, national and international entrepreneurs.
In 2011, Bill Muirhead and Charles Fontannaz, created VFM Conseil SA providing strategic consulting, audit and accounting & tax services.
In 2014, GMB Services SA was created to bring Engineering , Quality Assurance & Regulatory Affairs and Operational Excellence services, particularly to clients in the medtech and industrial sector.
We help you to concentrate on what is important for the development of your business
To make a great product, deliver a great service and build long-term business, you need to have the right vision, the right ingredients and the right people.
To succeed you need to be passionate and patient (not always…!).
To really understand our clients’ business and needs.
To challenge existing ideas to bring innovative solutions for our clients.
To work with entrepreneurs who are change-orientated, who are prepared to challenge the norm, to help them make transformative decisions to deliver success.
We are entrepreneurs, like our clients, who strive to be innovators, never satisfied with the status quo.
We are passionate about what we do and building long-term relationships with our clients.
We have a commitment to the highest quality, professionalism and excellence in everything we do.
We strongly believe in ethical standards in everything we do.
We are not afraid to say what we think. Tell it like it is in a direct and straight-forward manner.
Our experts who provide engineering and consulting solutions.
CEO / Senior Consultant
Senior Engineering, QA/RA & Business Excellence Expert
Bertrand Gabry has a Materials Science and Engineering PhD from the University of Franche-Comté and a degree in Mechanics and Production from the University of Bourgogne.
He is a team leader with extensive experience in his field, the ability to assess the operational organization, and the ability to provide pragmatic and effective solutions to complex problems.
Previously, he was responsible for the Spine Business Unit, Group Quality & RA Manager of Valtronic Technologies, Quality Manager of AP Technologies and the Pneumatics Division of Parker Hannifin.
Bertrand has experience in the automotive, industrial, medical technology and luxury sectors.
He has expertise in management, engineering, project management and QA/RA.
He is also a Board member of a number of different companies.
Senior QA/RA & Continuous Improvement Expert
Frédéric Enggasser is an experienced Quality Manager with expertise in the medical device industry. He has previously worked during 14 years in manufacturing and in quality department, in a company developing and manufacturing electromechanical devices where he gained experience in manufacturing process validation (IQ,OQ,PQ), nonconformity and CAPA management, documentation for new product development, internal audit, Quality System Management and MDSAP preparation.
He successfully participates to several ISO13485 implementation and certification as well as FDA audit. Frédéric can, with his background and expertise, provides support for audits, documentation management, risk management and regulatory pathway.
Embedded Software & Electronics Engineer
Jérémie Macchi has an Bachelor’s degree in Electronics and Mechatronics and a Master in Industrial Technologies, with a specialization in the Embedded Systems field.
His expertise spanning from Digital and Analog Electronics to Embedded Firmware development.
He provides GMB’s clients his expertise for their R&D projects, feasibility studies, industrialization projects and all other projects requiring in-depth knowledge of the latest technologies.
Clinical, Regulatory & Human Factors Engineer
Marine Poyard is a biomedical engineer. She has 4 years of experience in Regulatory and clinical affairs. She worked has regulatory and clinical associate for neurotechnology startup company. This role was to implement the regulatory and clinical process for neurological medical device.
This background allows her to have a knowledge of the requirements to put a medical device on the market. Marine is ready to provide support in the following fields: regulatory requirements for CE mark (applicable standards, medical device classification, V&V….), clinical evaluation report, literature review, usability engineering file, quality management systems.