Inventory Specialist I

About the Company

Ratio Therapeutics is committed to improving and extending the lives of cancer patients without sacrificing their quality of life. We are a team of passionate scientists, engineers, and business professionals dedicated to advancing the field of targeted radioligand therapy. Our proprietary TRILLIUM and MACROPA platforms enable fine-tuning of radioligand pharmacokinetics and simplify the manufacturing process for the alpha-emitting isotope, actinium-225. These technologies have resulted in an emergent pipeline of novel therapeutic candidates.

Responsibilities

• Manage receipt, inspection, quarantine, release, storage, and issuance of raw materials, components, and consumables.
• Maintain accurate inventory records in the ERP system and ensure lot/batch traceability.
• Perform cycle counts, inventory reconciliation, and investigate discrepancies.
• Manage material ordering and replenishment to avoid stockouts or excess inventory, including radioactive isotopes.
• Ensure materials are stored per required GMP, GDP, and manufacturer’s conditions such as temperature, segregation, status labeling, and expiration control.
• Monitor expiry and retest dates to coordinate disposition of expired, obsolete, or damaged materials.
• Support inventory audits, inspection, and compliance.
• Prepare and support regulatory inspections by the FDA, EMA, and other health authorities.
• Create, review, and revise related documents, including SOPs and forms.
• Participate in quality systems activities, including change controls, CAPAs, deviations, and investigations.

Requirements

• Bachelor’s degree in supply chain, logistics, business, life sciences, or related field.
• 2+ years of inventory, warehouse, materials management, or logistics experience. GMP experience preferred.
• Working knowledge of cGMP, GDP, and material traceability requirements.
• Strong attention to detail and ability to follow written procedures and maintain inspection-ready documentation.
• Ability to work safely in a manufacturing and warehouse environment and follow site EHS requirements.
• Strong organizational, communication, and cross-functional skills.

This role will support the buildout and phased expansion of our new radiopharmaceutical manufacturing facility in the Salt Lake City metropolitan area (West Valley City, Utah) and GMP manufacturing operations once the site is operational.