Your Responsibilities

· Build up of Quality Management Systems according applicable MedTech standards (e.g. ISO 13485, ISO 14971, MDR, IEC 62366, IEC 62304)

· Execute projects for costumers independently (usually on customer's site) regarding support for Quality Management Systems

· Problem solving and solution finding with right balance between quality, compliance, and business needs

· Advice and consult customer (take indirect leadership as appropriate)

Your skills and experiences

· At least 10 years' experience in building, maintaining, and operating Quality Man-agement Systems according to applicable MedTech regulations and standards, in-cluding experience in relevant regulation for EU and US.

· Experience and knowledge in eQMS are welcome

· Education in engineering or natural science, at least Master of Science (MSc) - background in electronic and firmware development is welcome

· Independent & self-organized

· Systematic & analytical thinking, process oriented and risk based

· Hands-on attitude

· Strong decision maker, takes the lead where appropriate and necessary

· Ability to gain the trust of various stakeholders, from shop floor to management

· Fluent in English and German

Your benefits

· You will work in the Zurich area for an ambitious, dynamic small company in the medical technology sector with a very good working atmosphere

· You benefit from flexible working hours and an exciting and versatile field of activity

· You work in a company with a flat hierarchy, short decision-making processes

· You can expect a pleasant working atmosphere, an uncomplicated and collegial co-operation

· You benefit from modern and attractive working conditions and development oppor-tunities

· An attractive salary and very good social benefits round off the offer