CDMO Materials Management Manager
Lantheus## Company Overview
Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease for better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and the United Kingdom, Lantheus has been providing radiopharmaceutical solutions for near
...
ly 70 years.
Today, we are expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions and strategic partnerships across the life sciences ecosystem, we are accelerating efforts to advance precision medicine and improve patient outcomes worldwide.
At Lantheus, we are purpose-driven, and every employee plays a vital role in our success. We are dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.
## Summary of Role
We are seeking a CDMO Materials Management Manager. This role is responsible for overseeing the accuracy, control, reconciliation, and reporting of inventory across radiopharmaceutical development, manufacturing, quality control, warehouse, and distribution operations. The manager ensures that GMP materials, radioactive materials, APIs, precursors, reagents, components, finished radiopharmaceutical products, cold kits, labels, and consumables are received, stored, counted, replenished, transferred, and reconciled in accordance with cGMP, GDP, radiation safety, DSCSA, DOT/IATA, company procedures, and applicable regulatory requirements.
This position is based in New Jersey and requires on-site presence five days per week. It is open to applicants authorized to work for any employer within the United States.
## Responsibilities
- Lead day-to-day inventory control activities for GMP and non-GMP materials, including receiving support, put-away verification, stock movement, cycle counting, physical inventory, and reconciliation between physical inventory and inventory management systems.
- Maintain accurate inventory records for raw materials, excipients, APIs, radionuclides, precursors, reagents, components, labels, packaging materials, finished goods, kits, PPE, cleaning supplies, and other controlled materials.
- Ensure inventory transactions are completed accurately and timely in applicable systems such as PETra, SAP, ERP, WMS, eQMS, or other site inventory platforms.
- Manage inventory controls for temperature-sensitive, time-sensitive, short shelf-life, and radioactive materials, including lot, expiration, calibration, activity, storage condition, and chain-of-custody requirements.
- Coordinate routine cycle counts, quarterly physical counts, variance investigations, and inventory reconciliations; document discrepancies and drive timely resolution with Supply Chain, QA, QC, Manufacturing, Finance, and Warehouse teams.
- Establish and monitor inventory levels, reorder points, safety stock, expiry controls, and replenishment plans to support uninterrupted manufacturing, QC testing, clinical supply, commercial distribution, and customer commitments.
- Support quarantine, release, hold, rejected, expired, returned, recalled, damaged, or suspect product processes in partnership with Quality Assurance and Regulatory/Compliance teams.
- Ensure compliance with cGMP, GDP, DSCSA, PDMA, applicable state licensing expectations, DOT/IATA hazardous materials requirements, radiation safety procedures, and internal SOPs.
- Partner with Procurement and Planning to prevent stockouts, excess and obsolete inventory, material shortages, and avoidable production or shipment delays.
- Develop, maintain, and improve SOPs, work instructions, checklists, training materials, and inventory control processes.
- Support internal audits, customer audits, regulatory inspections, and management reviews by providing inventory reports, reconciliation evidence, deviation support, and corrective action updates.
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