Inventory Specialist I

Ratio Therapeutics, Inc.•West Valley City, UT

6d•Onsite

About The Position

Ratio is seeking an Inventory Specialist I to support the buildout and phased expansion of our new radiopharmaceutical manufacturing facility in the Salt Lake City metropolitan area (West Valley City, Utah) and to support GMP manufacturing operations once the site is operational. This role will focus on inventory and material management to support operations of the facility including manufacturing and laboratory materials and standards. The ideal candidate will enjoy working in a collaborative, fast-paced, multidisciplinary environment.

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

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 the 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