inmedis GmbH is a successful and established consulting company for quality management and regulatory affairs in medical technology. Our customers value us as business partners who are familiar
with current regulatory requirements and can implement lean and pragmatic solutions. For our further growth, we are looking for a professional who strengthens our young and uncomplicated team.
You have at least 5 years of experience in the medical device industry, preferably in quality engineering or in development.
You work independently and structured.
You can express yourself correctly in German and English, spoken and written.
You always find customer-oriented and practicable solutions.
Continuing education goes without saying for you.
You act safely and competently in every situation.
You enjoy using Microsoft's latest IT tools.
Advise customers on questions about quality management and regulatory affairs.
Accompany projects as a quality engineer from product idea to post market surveillance.
Creation and maintenance of technical documentation (STED, DHF, DMR, DHR)
Creation of process descriptions, templates, checklists etc.
An exciting and varying field of activity.
Shaping the growth of our company.
Good work-life balance.
A highly motivated and uncomplicated team.
Appreciation is a top priority for us and we live it.
Continuing professional education and personal development.
A comfortable office in a central location in Zug.
We look forward to hearing from you by e-mail or phone +41 41 725 36 80.
