Role Description- You will audit compliance with ISO 13485 and CE marking regulations (Assessment of Conformity EC Directive 93/42/EEC) for medical devices as well for any other quality assurance systems for which you are qualified - You will present our certification services to potential clients and ensure the coordination of certification procedures - You will provide assistance for the implementation of new guidelines regarding accreditations - You will provide assistance for the development and implementation of our regulations in the field of certification - You will provide assistance for the further market development of our services for the assessment of medical devices and/or labour & environmental management systems - You may occasionally be required to carry out an assignment abroad
Responsibilities- You have a university or higher non-university qualification (e.g. Industrial Pharmacist, etc.) - You have at least 5 years of relevant professional experience in the medical or paramedical sector or as a safety & environmental manager - You have a thorough knowledge of the relevant legislation - You also have an in-depth knowledge of systems such as ISO 13485 - You have excellent interpersonal and communication skills at all levels - You have a good command, both verbal and written, of Dutch, French and English - You like to work in a meticulous manner and have good organisational skills
Requirements- An exciting position in an international group - You will work with a dynamic and professional team of auditors - A salary commensurate with your experience and expertise, supplemented with a company car
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.