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Regulatory Affairs Manager (Medical Devices)

  • Job type: Permanent
  • Location: Lorsch
  • Salary: Competitive
  • Job reference: RNMR
  • Sector: EPM Scientific, Regulatory
  • Date posted: 17/11/2017

My client is a leader in the medical device/biocides market. They offer a unique opportunity to work in a dynamic role, where the innovation is driven by customer needs. You will be working closely with the development team to efficiently bring products to market. 

Your tasks:
- Perform and maintain worldwide product registrations 
- Monitor compliance in accordance with 93/42/EEC directives and the necessary standards
- Participate in development projects, change management, PMS, risk analyzes and clinical assessments
- Control contact with authorities and authorities
- Optimise processes for efficient approval of medical devices and biocides

Your profile:
-  Medical, natural or engineering science degree
- Relevant knowledge of regulatory affairs (medical devices) - biocides authorisation desirable.
- Professional project management 
- Fluent German and English 

Interested, or know someone who might be? Apply by submitting your CV, or get in touch with me via email or phone.
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