Drug Regulatory Affairs Manager (m/f/d)

Zugo | Freie Mitarbeit 
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Kategorie(n): Gesundheit
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Projektbeschreibung

Referenznummer: 464480/1
Startdatum: asap
Projektdauer: 4 MM
Ort: Zugo

Meine Aufgaben:
  •  Preparation of the regulatory strategy for new submissions
  •  Timely submission of new products to Swissmedic in agreement with the yearly target
  •  Obtain a number of marketing authorizations in accordance with the yearly target
  •  Drive product maintenance to ensure regulatory compliance.
  •  Provide close regulatory support to the product launch work stream
  •  Strategic business partner to Business Development, Quality Assurance, Supply Chain as well as
  • For other Global Regulatory Groups (RCCs)
Meine Qualifikationen:
  • Education: Pharmacist or natural scientist preferably with medical background
  • Languages: German (fluent), English (intermediate to advanced)
  • Experience: Intermediate profound Regulatory and Drug development experience
Meine Vorteile:
  • Professional and trusting cooperation
  • We will create a candidate profile containing your strengths and potential and thus increase your chance of being placed in a position
Über Hays:
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.


Einsatzort: Zugo

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