Jobs at Lantheus

Serve as on-site CDMO contracts and operations lead: manage client/vendor MSAs and work orders, oversee budgeting, billing, resource allocation, procurement, and cross-functional coordination to support CDMO projects and site strategy.

Lead MSAT activities for internal and external manufacturing partners, managing tech transfers, process validation, deviations/CAPAs, change controls, and lifecycle management. Supervise and mentor MSAT staff, collaborate with Quality, Manufacturing, Regulatory and Supply Chain, support audits/inspections, and drive process robustness and continuous improvement in a cGMP-regulated radiopharmaceutical environment.

Architect and govern hybrid infrastructure across on-prem, colocation, and multi-cloud environments. Lead M365, identity (Okta), endpoint (Intune/SCCM/Tanium), DR (Rubrik) and AI-driven automation initiatives. Partner with security and vendors, drive cost optimization, and translate business needs into resilient infrastructure roadmaps.

The CMMS Specialist manages the Computerized Maintenance Management System to support maintenance, utilities, and compliance in a pharmaceutical setting, ensuring accurate data and effective processes.

The Market Access Leader will engage with key decision makers and stakeholders to ensure favorable access for Lantheus' products, addressing reimbursement issues and collaborating across functions to support business goals.

The role involves leading commercial analytics for the Prostate Cancer franchise, analyzing sales data, providing insights, and collaborating cross-functionally to support brand strategy. Key responsibilities include executing analytics projects, managing external vendors, and communicating findings to stakeholders.

The Commercial Analytics Associate Director will analyze brand performance, deliver insights, and lead analytics projects to support strategic decisions across commercial operations.

The Associate Director will partner with commercial teams to generate market insights and support the commercialization of cardiac products, utilizing market research and competitive intelligence.

Oversee and administer corporate document control within Quality Systems, managing lifecycle of controlled GxP documents in TrackWise Digital. Support eDMS projects, validation, migrations, inspections/audits, training, metrics, remediation, and process improvements while ensuring regulatory compliance and governance across global sites.

Lead regional clinical application efforts for radiopharmaceutical products by building KOL/HCP relationships, providing training and technical expertise, supporting field research and clinical trials, ensuring regulatory compliance, and representing the company at scientific meetings.

Lead and improve order-to-cash systems and processes, supporting SAP S/4HANA OTC modules, integrations (APIs/EDI), and vendor partnerships. Drive KPI-based performance, root-cause analysis, process improvements, compliance (GDP, SOX), issue resolution, reporting, and cross-functional coordination for billing, revenue integrity, and new product/system launches.

Manage supplier quality lifecycle for domestic and international suppliers (CMOs, APIs, raw materials, 3PLs). Serve as primary contact for 3PL/pharma partners, oversee supplier performance, lead supplier qualification/onboarding, handle deviations and CAPAs, support supplier change control, audits, and metrics reporting, and drive continuous improvement to maintain compliant vendor management and supply risk mitigation.

Lead market access strategy and execution for major IDNs, academic centers, and large groups to secure coverage, coding, reimbursement, and site setup for current and upcoming radiopharmaceutical products. Build senior relationships, resolve reimbursement issues, drive pull-through, execute educational programs, run business reviews, and collaborate cross-functionally to support patient access and product launches. Field-based with significant travel.

Lead clinical study design, protocol development, and interpretation through IND to registration. Serve as clinical lead across cross-functional teams, author key study and regulatory documents, oversee study execution and safety reporting, engage investigators and KOLs, support publications and advisory meetings, and drive clinical strategy for radiopharmaceutical and oncology programs.

The Market Access Director will lead access strategies for Lantheus' products, build relationships with key accounts, and drive brand growth through education and collaboration with health systems and payers.