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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.