The preparation of the scientific documentation for the performance evaluation and the preparation of the Technical documentation for submission to our Notified Body

Recording and implementation of product requirements with regard to the IVDR (EU Regulation 2017/746)

Conducting post-tests and analysing the performance evaluation

Scientific approach to state of the art implementation

Carrying out risk assessments for our products in accordance with IVDR requirements

Specialities:

You will become a subject matter expert in the various product lines and with regard to the IVDR

You will make a significant contribution to maintaining the supply of IVDs in Europe

You have successfully completed your Master‘s degree in natural sciences, e.g. biology, biochemistry, molecular life science or similar, you have successfully completed

It is easy for you to grasp complex issues quickly and to formulate them concisely and comprehensibly and understandable, for documentation you use your knowledge of MS Word and Excel

You are a team player and have strong communication and organisational skills

Your excellent language skills in English and German will help you when creating documents

You are a team player who works with a lot of initiative and independence for the IVDR product transfer

Full-time permanent employment contract with 31 vacation days per year

Flexitime with working time account; no shift and weekend work

Flat hierarchies and a cooperative atmosphere in a medium-sized company

Coffee and fresh fruit every week

Health workshops

Contributions to the company pension plan

Regular in-house training

Job bike