Teams at JAMP Pharma Group

Supports the issuance, revision, implementation, and maintenance of commercial finished-product specifications for pharmaceutical drugs and natural health products. Coordinates with partners and suppliers to obtain product specifications, analytical methods, and validation evidence. Reviews change requests affecting specifications, supports new product launches and technology transfers, and updates internal specifications. The role requires a science student with basic GMP knowledge and French-English bilingual communication skills.

Conducts pharmacovigilance, product safety surveillance, and risk management for marketed pharmaceutical products in Canada and internationally. Responsibilities include medical review of adverse event reports, causality and seriousness assessment, safety signal detection and analysis, risk management plans, PSUR/PBRER review, benefit-risk evaluations, and assessment of regulatory requirements. Requires pharmacy or medical training, pharmacovigilance experience, knowledge of Health Canada, ICH, and GVP guidelines, Argus Safety experience, and French-English bilingual communication.

Soutient l’évaluation et la gestion des plaintes qualité liées aux produits pharmaceutiques. Participe à l’évaluation des risques, à l’examen des rapports d’investigation des fabricants, à l’analyse des tendances et à l’identification des partenaires présentant des difficultés. Le poste implique également l’examen des échantillons de plaintes et de rétention, sous la supervision de l’équipe Investigations et Plaintes.