Senior Vigilance and PMS Specialist
Salary/Rate:70,000EUR - 85,000EUR
Job type:Perm
Town/City:Munich
Country:Germany
Business Sectors:Regulatory Affairs, Quality
Job ref:25101
Post Date:15. 04. 2024
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About the Role
Senior PMS & Vigilance Specialist
Are you a competitive spirit, looking for the next challenge to conquer?
Do you believe that effective teamwork can propel you further than you could ever go by yourself?
Are you looking for a future-proof workplace where personal and appreciative cooperation is at the core of your employer’s mission?
Look no further…
Overview:
My client is an industry leader in orthopaedic product development and medical education. They are dedicated to delivering top-quality solutions for healthcare professionals and the countless patients benefiting from their devices.
Tasks:
Your Profile:
Interested?
Please apply with your CV or contact Vivien Zsuzsanna Urban for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management.
vivien.urban@adaptivelifescience.com
+49 30 16639819
#LI-VU1
Are you a competitive spirit, looking for the next challenge to conquer?
Do you believe that effective teamwork can propel you further than you could ever go by yourself?
Are you looking for a future-proof workplace where personal and appreciative cooperation is at the core of your employer’s mission?
Look no further…
Overview:
My client is an industry leader in orthopaedic product development and medical education. They are dedicated to delivering top-quality solutions for healthcare professionals and the countless patients benefiting from their devices.
Tasks:
- Creation and submission of vigilance reports in the EMEA region
- Assessment of potentially reportable incidents
- Processing product complaints, monitoring and coordinating further processes
- Handling FSCAs
- Participating in internal and external audits
Your Profile:
- Degree in a scientific, medical or technical field or comparable qualification
- Experience working with medical devices or similarly regulated products
- Sound knowledge of handling customer complaints and reportable events per MDR
- Knowledge of additional international medical device regulatory frameworks are a plus! (e.g. FDA, MDSAP etc.)
Fluent written and spoken German and English are a must!
Interested?
Please apply with your CV or contact Vivien Zsuzsanna Urban for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management.
vivien.urban@adaptivelifescience.com
+49 30 16639819
#LI-VU1