Reporting to General Manager according the business management & strategy. 35% yearly growth milestones.
monitoring all the business areas, but focus in Safety and electromagnetic compatibility (EMC) compliance based on testing and certification for renewable energy installations and components.
Field of expertise: Safety and EMC compliance business areas & international Markets
- Since 2018 - Business Manager at CERE
- 2013-2018 - Sales Manager of the E&E Testing Laboratory at SGS
- 2010-2013 - Technical-Sales Notify Body´s and Laboratory´s Services on Medical Device product at SGS
- Latest - Graduate Environmental Science
- Graduate Environmental Science in Alcala de Henares University of Madrid, Spain.
Nowadays, and for the last 2 years, Ruben has been working in CERE as Business Manager of the testing laboratory in terms of electromagnetic compatibility and safety compliance.
On his background, he has managed different testing and certification projects, working with more than 1.000 different manufacturers.
During these years, he has also been working on strategic plan to increase the business with news fields and scopes of CERE as testing laboratory and certification body, and always related with electrical and electronic devices. This fields are mainly electric vehicle supply equipment, industrial machinery, IT equipment, medical devices, and household appliances.
These new field involve some business support mainly in exhibitions. In the commercial area, apart from attending Clients and incoming projects during the quotation stage, he has visited and attended MEDICA Exhibition in Germany since his incorporation to CERE's team.
Previously and before joining CERE, he worked at SGS for 11 years. He started as a salesperson, after 3 years he became Technical-Sales Notify Body´s and Laboratory´s Services on Medical Device product. After 6 years he became the Sales Manager of the E&E Testing Laboratory with a team of 5 people and responsible of the management of all the business.
Ruben's field of expertise can be considered the regulation of compliance concerning Medical Device around the world.