Director Medical Services
3 weeks ago
Poste en mode hybride avec horaire flexible;
~ Poste régulier et à temps plein;
~ Bureau à proximité de la station du DIX30 du REM;
~ Relevant du Vice-président des affaires scientifiques et développement des affaires, le/la Directeur(trice) des affaires scientifiques assure la direction du groupe scientifique composé des départements Qualité, Réglementaire et Pharmacovigilance. Superviser le Gestionnaire principal des affaires réglementaires, la Gestionnaire contrôle qualité, le Gestionnaire assurance qualité ainsi que la Chef pharmacovigilance et information médicale;
Établir et exécuter des stratégies pour une amélioration continue et efficace du groupe scientifique et des projets;
Assurer la formation adéquate du personnel du groupe scientifique, notamment en approuvant les plans de formations, descriptions de postes et en offrant des formations externes et du support à l’interne;
Assurer que les activités qualité de l’entreprise sont faites en conformité avec les bonnes pratiques de fabrication (BPF) et toutes autres réglementations pertinentes;
Assurer que les ententes qualités sont mises en place avec la coopération et l’expertise du Gestionnaire en assurance qualité, au besoin;
plan de gestion des risques, monographie de produit, RMP), au besoin;
en matière de qualité, réglementaire, pharmacovigilance et veiller à ce que l’entreprise les respecte, en collaboration avec les secteurs fonctionnels intéressés.
Détenir un diplôme d’études supérieures (p. ex. maîtrise ou doctorat) en pharmacie, biochimie, chimie, microbiologie ou un autre domaine scientifique connexe;
Expérience en gestion d’équipes;
Bilinguisme (français et anglais) afin de pouvoir communiques avec les employés en Ontario et les partenaires à l’extérieur du Québec;
Excellente connaissance et maitrise du concept qualité, des processus de fabrication, de la nature des produits pharmaceutiques, des pharmacopées et des réglementations BPF;
Habileté informatique avec la suite Microsoft Office.
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