Associate Director, Procurement, Summit Site Lead

Major Responsibilities and Accountabilities

• Ensure continuity of direct material supply for cGMP manufacturing by managing suppliers and engaging site stakeholders and global support teams.
• Capture strategic value at the site level (spend segmentation, risk identification, supplier renegotiation).
• Ensure value capture visibility via Sievo and bi‑weekly leadership updates.
• Lead Supplier Relationship Management with Site GM in alignment with Category Leads and site stakeholders.
• Achieve metrics: value beyond savings, PPV, RTP, inventory, and invoicing compliance.
• Standardize raw materials/consumables and drive cost savings via alternate/secondary sourcing.
• Develop and execute regional sub‑category and capital investment strategies with compliance/governance.
• Lead sourcing events and the annual site operations budget process for locally sourced and indirect materials.
• Support cGMP/finance audits; escalate supply‑related audit requests; lead risk assessments and business continuity.
• Manage procure‑to‑pay transactions, enforce policies/internal controls, and govern sourcing approvals.
• Oversee contract management and support LOIs, SOWs, and MSAs.
• Recruit, manage, and develop procurement operations personnel.

• Education:
  
  B.S./B.A. in science, engineering, or business.
• Experience:
  
  7+ years multi‑disciplined procurement; preferred technical/operational/business background and highly preferred prior cGMP in biopharma/pharma/medical devices.
• Preferred: SAP and/or other ERP systems.
• Skills:
  
  problem‑solving, cross‑functional collaboration, strong analytics/interpersonal/communication/negotiation, customer service orientation, independence with minimal senior supervision.

• Health coverage (medical/pharmacy/dental/vision), wellbeing support (EAP and wellbeing programs), and financial protection (401(k), disability, life insurance, etc.).
• Paid time off, including flexible/unlimited time off for US exempt employees.