My client, a Global Medical devices company are looking for a Regulatory Manager based in Baden-Württemberg.
A great opportunity to join a fast-growing company with a great portfolio of products and clients.
Salary: Up to 65,000€
- Preparing and implementing the MDR
- Being Responsible for Technical Documentations
- Implementing QMS to ISO 13458:2016 or MDSAP
- Close interaction with international Notified Bodies and Competent Authorities
- Setting up risk management
To be considered you need to have
- Eligibility to work in Germany
- 2+ years’ experience in medical devices industry
- MDR experience desirable
- Excellent communications skills
- Fluent in English
Looking but this isn’t the right position for you?
If you are interested in a new opportunity but your experience doesn't fit this role, please email your CV and the best time for a call to to setup a confidential discussion about potential opportunities.
Catalyst Life Sciences
CLS are a global recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas.
RA / regulatory / MDD / MDR / devices / 13485 / submission / regulatory / FDA / CFR / 21 / MDSAP / MDR / project / manager / CE / marking / QMS / SOP / technical / files / documentation / Risk / medical
We aim to be an equal opportunity recruiter and we are determined to ensure that no applicant receives less favourable treatment on the grounds of gender, age, disability, religion, belief, sexual orientation, marital status, or race, or is disadvantaged by conditions or requirements.
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