20/01/2017

[Empleo] International Regulatory Affairs Manager EMEA & USA

New position to support the company in its strategy of growth and products launching.

Position based in the Global Headquarters in Paris, France. A flexible organization is possible.

Reports to the Head of Global Market Access, based in the Global HQ.

Stakes:

– Be an actor of the company’s market access strategy

– Propose and implement the regulatory strategy for EMEA & US.

Position assets:

  • Company :

  • A world leader in animal nutrition

  • Strong notoriety in the market

  • Profitability and solid growth dynamics

  • Belongs to an international group with clear and high ambitions in animal nutrition

  • Strong commitment to innovation and HR Development. High team spirit

  • Human sized company: International company with the proximity of a mid-size company

  • Global headquarters close to Paris and global presence allowing a wide range of future evolutions.

  • Position:

  • Newly created position

  • Complete position: strategic and operational

  • High level of responsibility and autonomy

  • Transversal position in direct and close interaction with all professions and directions of the company

  • Within a dynamic and highly cohesive team, key actor in the development strategy of the company.

Researched profile:

  • Scientific Education in Life Sciences:

Agronomy/ Agriculture Engineer Nutritionist, or DVM (Doctor in Veterinary Medicine), or Master in Animal Health & Nutrition…

  • Minimum 3 years’ experience in Regulatory Affairs or Regulatory Compliance:

  • In Industry: Animal Nutrition, Plant protection, Animal Pharmaceuticals, Food,

  • In a Consulting business in Regulatory Affairs,

  • or Assessor within a Regulatory Agency in animal health.

  • Required skills :

  • Understanding of regulatory and legal framework

  • Knowledge in animal nutrition through experience in R&D, Formulation…

  • Positive factors:

  • International profile: Education and /or experience at international

  • R&D experience in elaborating protocols of clinical studies

  • Writing regulatory files. 

  • Languages: Fluent in English (oral & written). French is a plus.

Contact Dr Véronique DUGUÉ, GIUDICELLI INTERNATIONAL Executive Search: vdugue@giudicelli-international.com