Clinical Evaluation Specialist (m/f/d)

REFERENCE NUMBER:

619493/1

MY DUTIES:

- Responsible of the medical device risk management process (according to ISO 14971)
- Work in interdisciplinary and multinational teams to create better and robust products and solutions and run the testing activities within various teams
- Planning and conduction of Clinical Evaluations
- Process, selecting PMCF methods, designing PMCF studies, execution of PMCF activities, and reporting of PMCF in accordance with MDR and FDA regulations

MY QUALIFICATIONS:

- Experience in the field of medical device industry
- Experience with risk management according to ISO 14971
- Experience with IEC 62304, IEC 62366 and FDA guidance documents is beneficial
- Strong knowledge of MDR, FDA, and Good Clinical Practice
- Fluency in English and German

MY BENEFITS:

- Interesting tasks in an international environment

ABOUT HAYS:

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.