CDMO Materials Management Senior Specialist

Requisition Number: CDMOM
003924

• Posted :
  September 1, 2026
• Full-Time
• On-site

Showing 1 location

Springfield, NJ, USA

Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years.

Today, we’re expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.

At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We’re dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.

Join us and be part of a company where your contributions make a real impact, because we know someone’s health is in our hands.

Summary of role
We are seeking a CDMO Materials Management Senior Specialist. The Materials Management Senior Specialist is responsible for overseeing the accuracy, control, reconciliation, and reporting of inventory across radiopharmaceutical development, manufacturing, quality control, warehouse, and distribution operations. This role 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 a presence on-site (five) days per week, and open to applicants authorized to work for any employer within the United States.

• 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.
• Lead or support deviations, CAPAs, change controls, investigations, and process improvement initiatives related to inventory accuracy, material traceability, system controls, and warehouse compliance.
• Prepare and communicate inventory metrics, aging reports, expiry risk reports, material availability updates, inventory valuation support, and operational readiness dashboards for leadership and cross-functional stakeholders.
• Train, coach, and provide daily direction to inventory control specialists, warehouse associates, or cross-functional users involved in inventory transactions and material handling.
• Serve as primary point of contact for business development and operational needs for existing and prospective CDMO clients. Prepare work orders for…