Strategic Medical Device Buyer & Supply Chain Leader

Profound Medical; Mississauga; On-site; CAD 85,000 - 110,000; Full time

Job summary

Profound Medical is seeking a Senior Buyer to lead strategic procurement for direct and indirect materials, ensuring uninterrupted supply for medical devices. You will manage supplier relationships, negotiate contracts, and support regulatory compliance across GMP/ISO13485 environments.

You will collaborate with Manufacturing, Planning, Quality, Regulatory, and Engineering to optimize cost, lead times, and performance while maintaining documentation and data accuracy.

Qualifications

• 7+ years of purchasing, sourcing, or procurement experience in a regulated manufacturing environment.
• Experience with global suppliers and supplier negotiations.
• Knowledge of GMP, ISO 13485, FDA, Health Canada, and other regulated manufacturing requirements.
• ERP/MRP experience with SAP, Oracle, or Microsoft Dynamics.

Responsibilities

• Manage procurement activities for raw materials, components, subassemblies, packaging, and indirect spend.
• Execute purchasing transactions including purchase orders, supplier agreements, and contract renewals.
• Ensure timely availability of materials to support production schedules and customer demand.
• Monitor supplier delivery performance, lead times, and inventory levels to minimize supply disruptions.
• Lead sourcing initiatives to achieve cost savings and continuity.
• Collaborate with Quality Assurance on supplier qualification, audits, and compliance.

Skills

Procurement experience

Negotiation

Analytical skills

Excel / data analysis

Education

Bachelor's degree in Supply Chain/related

CPM / CPSM / SCMP or equivalent certification

Tools

SAP

Oracle

Microsoft Dynamics

Job description

Profound Medical is seeking a Senior Buyer to lead strategic procurement for direct and indirect materials, ensuring uninterrupted supply for medical devices. You will manage supplier relationships, negotiate contracts, and support regulatory compliance across GMP/ISO13485 environments.

You will collaborate with Manufacturing, Planning, Quality, Regulatory, and Engineering to optimize cost, lead times, and performance while maintaining documentation and data accuracy.