CDMO Materials Management Senior Specialist

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 were 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. Were 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 someones 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.

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.
• 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 execution with existing and prospective customers.
• Cross-functionally support all operational teams in the CDMO including manufacturing MSAT QC and QC among others.
• Lead and manage CDMO vendor relationships including establishment of Master Service Agreements and service contracts.

Basic Qualifications

• Bachelors degree in supply chain Logistics Business Life Sciences Engineering or a related discipline preferred; equivalent experience may be considered.
• Minimum of 58 years of experience in inventory control warehouse operations supply chain materials management or logistics within a regulated pharmaceutical biotechnology radiopharmaceutical nuclear pharmacy medical device or GMP manufacturing environment.
• Prior lead or supervisory experience preferred including coaching employees assigning work resolving issues and supporting performance expectations.
• Strong understanding of cGMP GDP material traceability lot control expiration management quarantine controls inventory reconciliation and audit readiness.
• Experience handling or supporting temperature-sensitive short shelf-life hazardous or radioactive materials is strongly preferred.
• Working knowledge of ERP WMS inventory or manufacturing systems such as SAP PETra Oracle Microsoft Dynamics Blue Mountain Qualio or similar platforms.
• Familiarity with DSCSA DOT/IATA hazardous materials shipping radiation safety practices and controlled distribution environments preferred.
• Demonstrated ability to investigate inventory discrepancies identify root causes implement corrective actions and improve process controls.
• Strong communication organization analytical problem-solving and cross-functional collaboration skills.
• Ability to work in a fast-paced time-sensitive environment where product availability patient impact compliance and shipment timing are critical.

Preferred Qualifications

• Outstanding verbal and written communication skills are necessary with proven strong leadership skills.
• Goal-oriented self-starter with an acute attention to detail. Must be team-oriented able to work independently and proactively and able to multitask. Lead others by building consensus.
• Well-grounded in drug development with extraordinary leadership competencies and the strategic business perspective needed to bring products forward and to maximize their commercial value.

Core Values

The ideal candidate will embody Lantheus core values:

• Let people be their best
• Respect one another and act as one
• Learn adapt and win
• Know someones health is in our hands
• Own the solution and make it happen

The pay range for this position is between $111000 and $185000annually.

Actual base pay offered may vary depending on a number of factors such as job-related knowledge skills and experience. Employees in this position are eligible for a discretionary performance-based cash incentive. Benefits for this position include a comprehensive health benefits package that includes medical prescription drug dental and vision coverage. Other offerings include life and disability benefits pre-tax accounts a 401(k) with company contribution and a variety of other addition employees are eligible for a generous time off package including paid vacation holidays sick days and paid parental leave. Interested candidates can apply at . Applications for this position will be accepted until September 27 2026.

Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons actual or perceived race color creed religion national origin ancestry citizenship status age sex or gender (including pregnancy childbirth related medical conditions and lactation) gender identity or gender expression sexual orientation marital status military service and veteran status disability protected medical condition as defined by applicable state or local law genetic information or any characteristic protected under applicable federal state or local laws and ordinances.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition teamat .

Lantheus is an E-Verify Employer.

Applicants have rights under Federal Employment Law:Employee Polygraph Protection Act (EPPA);Family and Medical Leave Act (FMLA)
For California Applicants:Family Care & Medical Leave & Pregnancy Disability Leave;California Law Prohibits Workplace Discrimination & Harassment;Your Rights and Obligations as a Pregnancy Employee
For Ohio Applicants:Know Your Rights: Equal Employment Opportunity is the Law

Required Experience:

Senior IC