Regulatory Affairs Manager 100% (m/f)

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Beschreibung



Regulatory Affairs Manager 100% (m/f)

Reference: -en
Start: asap
Duration: 9 MM++

Main tasks:
  • Support of Regulatory Affairs Department for implementation of the requirements of the new In-vitro Diagnostic Regulation
  • Perform gap analysis for processes and products
  • Adapt processes and create templates
  • Generate and review related product documentation


Main qualifications
  • In-depth experiences in Regulatory Affairs and/or Quality Management for Design Control processes for In-vitro Diagnostic Medical Devices (ideal: background in instrument development)
  • Master degree or analogous in natural sciences, engineering, medicine or similar
  • Excellent English skills
  • MS Office


Main advantages:
  • A very renowned company
  • You will work in an international environment



About us:
With over 15 years of experience in the pharmaceutical industry, 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 professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

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Start
ab sofort
Dauer
9 MM++
(Verlängerung möglich)
Von
Hays AG
Eingestellt
17.01.2019
Ansprechpartner:
Kerstin Werner
Projekt-ID:
1702915
Vertragsart
Freiberuflich
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