Senior Director, Global Supply Chain & Device Manufacturing (IVDR)

Location: Hybrid role based in Boston, Massachusetts, US; organization spans the United States and Germany.

Salary: $224,880–$281,100 per year in the Boston, MA primary location; discretionary annual bonus may be available.

Company

hirify.global develops and operates regulated diagnostic laboratory services and products, partnering with Roche Diagnostics and external manufacturing partners.

What you will do

• Lead a global, cross-site team and set the strategy and operating model for supply chain, device manufacturing, and enterprise laboratory asset management.
• Build foundational capabilities, outsourcing and technology-transfer strategies, and a future-ready device manufacturing operating model.
• Own end-to-end supply of reagents, consumables, kits, and materials, including S&OP governance, inventory strategy, and material readiness.
• Manage laboratory equipment lifecycle activities, including capital assets, maintenance, calibration, service contracts, and compliance.
• Drive operational excellence, lean principles, continuous improvement, cost and capacity optimization, and transformational change across global sites.
• Ensure compliance with IVDR, FDA, quality systems, audits, documentation, CAPAs, and other applicable global regulatory requirements while partnering with Procurement, Quality, Regulatory, R&D, Lab Operations, and external partners.

Requirements

• Bachelor’s degree in Supply Chain, Engineering, Life Sciences, or a related field.
• At least 12 years of experience in a regulated industry, with progressive responsibility across supply chain, manufacturing, and/or laboratory operations.
• At least 5 years of people leadership experience, leading managers and teams in complex, matrixed environments.
• Experience leading global supply chain and/or regulated manufacturing operations across multiple sites and geographies.
• Experience owning end-to-end supply chain strategy and execution in clinical, diagnostic, or pharmaceutical environments, including R&D support and validation shipping protocols.
• Experience managing diagnostic kit, device, or reagent manufacturing operations at scale, including QC and distribution.
• Strong knowledge of cGMP, GDP, GCP, Annex 13, IVDR, QSR Design Control, and regulated manufacturing environments.
• Experience defining, implementing, or scaling ERP systems and integrated planning processes.
• Demonstrated program leadership, financial and analytical acumen, cross-functional influence, emotional intelligence, and the ability to lead teams through change.
• Understanding of HIPAA and the importance of protecting patient data and privacy.
• Ability to deliver results in a fast-paced, evolving environment without compromising quality or compliance.

Nice to have

• Master’s degree.

Culture & Benefits

• Lead a diverse global team with a culture of trust, inclusion, accountability, continuous development, and people-first leadership.
• Collaborate across a global operations leadership structure and with Roche Diagnostics and external manufacturing partners.
• Benefits are provided through hirify.global.
• The position is full-time and hybrid.