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Regulatory Affairs Manager - Biocides (m/f)


  • University degree in biology, chemistry, pharmacy, or equivalent
  • Solid background in Toxicology, Ecotoxicology, Environmental Science or Chemistry, Microbiology
  • At least 3 years' experience in the authorization of biocides in the international regulatory field (EU and worldwide), particularly with the Biocidal Products Regulation (EU) No. 528/2012
  • Providing advice and guidance to clients on EU and national data requirements according to the Biocidal Products Regulation (EU) No. 528/2012
  • Development of regulatory authorisation strategies for biocidal products (EU / Global)
  • Coordinating of project teams preparing authorization dossiers for biocidal active substance and biocidal products
  • Ensure that authorization projects are delivered on-time, within scope and within budget
  • Communication and close co-operation with our clients, CROs and authorities throughout Europe and on a global scale
  • Develop and maintain regulatory knowledge of European and worldwide (biocidal) regulations
  • Build-up, maintain and share practical knowledge in a fast growing, strongly team-oriented working group


» Job description


Employer:
Dr. Knoell Consult GmbH
Location:
68165 Mannheim
Part-time:
Yes


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