TÜV SÜD | Germany | 22xxx, 21xxx, 81xxx, 50xxx, 90xxx, 51xxx, 20xxx, 60xxx, 80xxx, 68xxx, 65xxx Frankfurt am Main, Hamburg, Köln, Mannheim, München, Nürnberg | Contractor position | Full time | Published since: 27.05.2026 on stepstone.de
Freelance trainer for the Medical Device Operator Ordinance (MPBetreibV) (m/f/d)
Since 1866 our passion for technology and safety has been valid. Innovations affect our lives in a variety of ways. For the safety of people and society, we renew each day and create confidence in new technologies. We are part of progress. We advise, we check, we certify. We act out of conviction, already today shape the world of tomorrow – set signs. We take the future into our hands. We are TÜV SÜD – more than 30,000 employees at over 1,000 locations worldwide. It is a special concern for us to take into account and promote any kind of diversity and speciality of people in the company. We look forward to applicants regardless of age, nationality, ethnic background, disability, gender and gender identity or sexual orientation, religion or worldview. Currently a freelance activity is to be awarded as Medical Device Manager (MPBettriebV) (w/m/d)
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Your tasks • Your profile • What we offer
You conduct seminars of the TÜV SÜD Academy on the Medical DevicesOrdinance (MPBettriebV) independent. With strong practical relevance, you can communicate your expert knowledge to: the regulatory requirements and their implementation with application-oriented examples the requirements, professional preparation and maintenance for safe operation the requirements of risk management, specific requirements and relevant special arrangements process steps along the entire product life cycle
You shall inform about the obligations of the participating actors (detection obligations, deadlines) and legal consequences in the event of violations of the rule. You continuously develop your technical knowledge and didactic skills to strengthen your coaching activity.
Medical (medical) technical or engineering degree or comparable qualification At least five years of professional experience in the environment of manufacturers, traders or operators of medical devices or in a designated body, focusing on medical device safety Very good knowledge in medical device law (legal and regulatory frameworks) Germany, as well as in QM according to ISO 13485 and the national laws and regulations: Medical Devices-EU Adaptation Act (MPEUAnpG) Medical Devices-EU Adaptation Regulation (MPEUAnpV) Medication law Vigilance System for Medical Devices Medical Device Law Implementation Act (MPDG)
Good rhetorical and didactic competence Experience with digital learning formats / online training
Didactic further education Exchange in our trainer network Access to seminars of the TÜV SÜD Academy
Location
 | TÜV SÜD | |
| 80331 Frankfurt am Main, Hamburg, Köln, Mannheim, München, Nürnberg | ||
| Germany |
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