Job Search and Career Advice Platform

Activez les alertes d’offres d’emploi par e-mail !

Deputy Local QPPV – PV Compliance France

Apsida Life Science

Montpellier

Sur place

EUR 40 000 - 60 000

Plein temps

Il y a 2 jours
Soyez parmi les premiers à postuler

Générez un CV personnalisé en quelques minutes

Décrochez un entretien et gagnez plus. En savoir plus

Résumé du poste

A leading biotechnology firm in Montpellier is seeking a Pharmacovigilance Support Specialist to aid the Local QPPV and ensure compliance with EU regulations. The role involves handling safety case management and supporting interactions with the French competent authority. Candidates should have a degree in Life Sciences and possess 2-4 years of relevant pharmacovigilance experience, with an understanding of French PV processes. This is an excellent opportunity to contribute to the stability and safety of innovative therapeutics.

Qualifications

  • Minimum 2-4 years of pharmacovigilance experience, preferably including EU PV requirements.
  • Experience working with French pharmacovigilance processes and local affiliates or distributors.
  • Exposure to audits or inspections is an advantage.

Responsabilités

  • Support to Local QPPV & Regulatory Compliance.
  • Act on behalf of the Local QPPV during absences, ensuring uninterrupted PV coverage.
  • Support interactions with the French competent authority (ANSM).
  • Escalate safety concerns and compliance issues promptly.

Connaissances

Regulatory compliance
Pharmacovigilance experience
Interaction with competent authorities
Safety concerns escalation

Formation

Degree in Life Sciences, Pharmacy, Medicine, or related field
Description du poste
A leading biotechnology firm in Montpellier is seeking a Pharmacovigilance Support Specialist to aid the Local QPPV and ensure compliance with EU regulations. The role involves handling safety case management and supporting interactions with the French competent authority. Candidates should have a degree in Life Sciences and possess 2-4 years of relevant pharmacovigilance experience, with an understanding of French PV processes. This is an excellent opportunity to contribute to the stability and safety of innovative therapeutics.
Obtenez votre examen gratuit et confidentiel de votre CV.
ou faites glisser et déposez un fichier PDF, DOC, DOCX, ODT ou PAGES jusqu’à 5 Mo.