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Regulatory Toxicology Expert


Détail de l'offre

Informations générales

Référence

2017-2822  

Date de parution

09/10/2018

Branche

Pharmaceutique

Société

INSTITUT DE RECHERCHE PIERRE FABRE SAS

Description du poste

Intitulé du poste

Regulatory Toxicology Expert

Contrat

CDI

Taux d'activité

Temps plein

Mission

Under the responsibility of the Director of Toxicology in our Pharmaceutical R&D department, you will act as a regulatory toxicology expert. The variety of your missions is enhanced due to the scope of our different activities (New Chemical Entities, biological entities, medication, food supplements, medical devices…) More specifically, your missions will include:
- Offering expertise within project teams from the set-up of our products' development plan through to their registration;
- Writing regulatory documents linked to your expertise;
- Ensuring follow-up of projects and corresponding research studies;
- Contributing to assessment of external opportunities;
- Producing analyses all along a product's lifecycle.

Profil

With a high-level scientific degree (PhD, pharmacist, veterinary…), we expect around ten years' experience in the pharmaceutical area.
Specialisation in repro-toxicology, veterinary anatomical pathology, antibody development or in assessment of food supplements or essential oils would be a plus.
You must have mastered GLPs and be renowned for your rigour, your commitment to customer service and your reactivity as well as your ability to anticipate.
You need to nurture innovation in a customer-service perspective and embody the company's humanist values.
Fluent English mandatory, fluent French is a plus.

Localisation du poste

Localisation du poste

Europe, France, Midi-Pyrénées

Lieu de travail

Toulous - Langlade (31)

Critères candidat

Niveau d'expérience minimum requis

8 ans ou plus

Langues

Anglais (4 - Courant)

Demandeur

Date de prise de fonction souhaitée

01/01/2019