Senior Corporate Compliance Auditor

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care. What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.

The Senior Corporate Compliance Auditor – Supplier & Risk provides pharmaceutical compliance oversight for audit activities, supplier qualification, risk management, and inspection readiness across McKesson Canada businesses. This role requires strong warehousing, distribution, 3-PL compliance expertise and the ability to interpret and navigate Health Canada expectations and applicable GXPs, Controlled Substances, Medical Devices, and corporate quality requirements into practical audit criteria, supplier controls, CAPA expectations, on a risk-based approach. The position acts as a compliance subject matter expert for internal, supplier, transporter, client, and regulatory audit activities, ensuring that audit records, supplier files, quality agreements, deviations, CAPAs, KPIs, and compliance trends are complete, accurate, defensible, and inspection-ready. The role also requires strong proficiency with digital technologies, data analytics, and AI-enabled tools to support compliance activities and continuous improvement. The Senior Corporate Compliance Auditor will perform the following activities: Compliance Oversight & Audit Execution Plan, lead, and execute internal (including but not limited to distribution center, Private Label, 3-P, PV, clinics), supplier, transporter, client, and regulatory-readiness audits, including compliance assessment, evidence review, reporting, observation classification, and CAPA follow-up in accordance with pharmaceutical regulatory and corporate requirements. Assess compliance with applicable regulations according to the specific activities performed or service provided. Ensure audit records are evidence-based, risk-classified, complete, and inspection-ready. Perform or oversee periodic risk assessments related to audit outcomes, supplier performance, quality events, CAPA effectiveness, and emerging compliance risks. Analyze audit findings, deviations, supplier issues, and CAPA data to identify trends, systemic occurrences, repeat observations, and opportunities to strengthen the quality systems. Maintain dashboards, KPIs, and compliance metrics for audit execution, supplier performance, CAPA effectiveness, overdue actions, and inspection readiness; provide risk-based recommendations to leadership. Create or revise SOPs, work instructions, templates, audit tools, checklists, and training materials to strengthen compliance controls and standardize practices. Provide practical compliance guidance and training on audit expectations, supplier oversight, documentation standards, CAPA quality, and inspection readiness. Effectively use and optimize digital quality tools, including audit/supplier systems (Master Control), dashboards, to improve compliance visibility, traceability, and efficiency. Recommend and implement digital compliance tools for efficacy and continuous improvement Supplier Compliance & Qualification Execute and maintain supplier lifecycle controls, including qualification, requalification, risk classification, monitoring, performance review, and periodic compliance assessment. Ensure supplier files are complete, current, and inspection-ready, including approvals, audit reports, CAPAs, and performance records. Evaluate supplier compliance risks related to regulated activities, outsourced services, transporters, storage, distribution, and quality-critical products