Elevate pharmacovigilance practices with Takeda as an Associate Director of International GVP Compliance in Toronto, Canada. Lead compliance strategies, drive inspection readiness, and ensure robust patient safety measures across key regions.As a crucial leader at Takeda, you will implement global GVP compliance strategies, serving as a subject matter expert in pharmacovigilance. Collaborating with local companies and safety stakeholders, you will strengthen the quality systems and drive continuous improvement initiatives.
Your expertise will be key in mitigating risks associated with pharmacovigilance compliance.Key Responsibilities:Lead GVP compliance initiatives across assigned regionsConduct compliance investigations and root-cause analysesManage regional inspection readiness and auditsProvide guidance on regulatory expectations and quality systemsIdentify and assess compliance risks for proactive managementRequirements:7+ years in pharmaceutical/compliance rolesStrong knowledge of GVP regulationsExperience with audits and inspectionsExcellent analytical and communication skillsRelevant scientific or health-related qualificationDrive regulatory compliance excellence and patient safety through strong leadership and cooperative methodologies.#J-18808-Ljbffr