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 regions
Conduct compliance investigations and root-cause analyses




Manage regional inspection readiness and audits
Provide guidance on regulatory expectations and quality systems
Identify and assess compliance risks for proactive management Requirements:
7+ years in pharmaceutical/compliance roles
Solid knowledge of GVP regulations
Experience with audits and inspections
Excellent analytical and communication skills
Relevant scientific or health-related qualification Drive regulatory compliance excellence and patient safety through solid leadership and team-oriented methodologies.

📌 Associate Director, Gvp Compliance Takeda Toronto
🏢 Takeda Pharmaceuticals
📍 Toronto