REGULATORY AFFAIRS MANAGER Infectious Disease/OTX CDD 9 months - Geneva

Lieu: Switzerland - Meyrin/Geneva

Fonction: Regulatory Affairs

Compagnie: OM Pharma

Marilda Martins

International Talent Acquisition Specialist

+41 58 851 67 69

Conditions pour les agences de placement

Votre profil

We are looking for a Regulatory Affairs Manager starting from October2018  for our OM Pharma site in Geneva to support regulatory affairs activities of the OM pharma portfolio. Your main responsabilities are the following:
  • Manage successful submissions for new marketing authorisations, renewals, variations and line extensions for various regions worldwide .Coordinate the responses to Q&A and ensure they are handled in a timely manner and in line with the approved product strategy
  • Responsibility for the designated regulatory projects with respective deadlines and forecasted budget, from regulatory assessment to strategy implementation
  • Collaboration with the CMC, International and submission groups to ensure appropriate planning and timely execution of the regulatory activities
  • Ensure compliance of dossiers with legislation and with the general requirements in respective regions
  • Support regarding preparation and handling of Aggregate Safety Reports (PBRER, RMP…) according to internal procedures
  • Interact with Regulatory authorities, partners and consultants
  • Interface with other departments on a national and international level
  • Ensure that changes are documented in accordance with internal procedures and are communicated in a timely manner to the Health Authorities
  • Ensure tracking tools and regulatory databases are maintained up to date
We are looking for a customer- and service-oriented person who brings experience in working with a wide variety of stakeholders across diverse teams both internally and with external partner companies. Furthermore, your profile meets the following criteria:
  • Scientific or Medical degree (pharmacy, chemistry or, biochemistry)
  • At least 5 years’ experience in Regulatory Affairs worldwide in within a pharmaceutical company
  • Fluent in English and French both written and spoken
  • Strategic thinking and acting, strong analytical and entrepreneurship skills
You describe yourself as a solution oriented and flexible person who enjoys working in an intercultural environment. Your work is characterized by its accuracy, a proactive approach and by the ability to work under stress and to deal with tight deadlines. Thanks to you strong communication and negotiation skills, you are able to lead projects successfully and to interact with senior stakeholders from different departments.

A propos de nous

Le Groupe Vifor Pharma, anciennement Groupe Galenica, est une entreprise Specialty Pharma mondiale qui se consacre à la recherche, au développement, à la fabrication et à la commercialisation de ses propres produits pharmaceutiques. Il est le partenaire de choix pour les solutions innovantes axées sur le patient. L’entreprise, qui entend devenir le leader mondial des traitements de la carence en fer et des affections néphrologiques et cardio-rénales, aspire à aider les patients du monde entier souffrant de maladies graves et chroniques à mener une vie meilleure et plus saine. Le Groupe Vifor Pharma possède des sites de production en Suisse et au Portugal, ainsi qu’un réseau dynamique de sociétés affiliées et de partenaires lui assurant une vaste couverture de marché dans le monde entier. L’entreprise affiche une présence mondiale en constante augmentation mais conserve de solides racines dans son marché d’origine, la Suisse.

Le Groupe Vifor Pharma est constitué de Vifor Pharma, de Vifor Fresenius Medical Care Renal Pharma – sa société commune avec Fresenius Medical Care –, de Relypsa et d’OM Pharma.

Pour plus d’informations, veuillez consulter notre site: http://www.viforpharma.com/fr/a-propos-de-vifor-pharma/qui-sommes-nous.

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Conditions pour les agences de placement