Capa Specialist (m/f/d)

You are a co-sponsored expert and central contact person for the process for troubleshooting and for the introduction of corrective measures (corrective and preventive actions). You support the identification of fault causes, the implementation of corrective measures and the subsequent effectiveness check. You ensure compliance with current normative and legal requirements and support the implementation of external and internal audits. You work across departments with different areas such as RA, R&D, production or purchasing.

You have completed university studies or completed vocational training and have over several years of professional experience in medical technology, preferably in the regulatory or quality environment. You have good knowledge of the relevant requirements (e.g. DIN EN ISO 13485:2016); MDR 2017/745; MDSAP, etc.) You already have professional experience in quality assurance and quality management. You have an interest and fun in cross-departmental work and are characterized by a responsible, structured, responsible, communicative and targeted way of working. You have very good knowledge of German and English in word and writing.

It is our agile and value-adding corporate culture with flat hierarchies and short decision-making paths that distinguish our dynamic and efficient work. All areas of responsibility act independently, characterized by our startup mentality combined with the structure and power of an established company. Through flexible working hours, regular team events, training and training opportunities, you can advance your development according to individual needs. .