of Role The Associate Director of Demand Planning for Pharmaceutical and Clinical Planning is responsible for ensuring the efficient coordination of demand forecasts, and collaboration with various stakeholders including commercial, quality assurance, internal manufacturing, and clinical teams to drive Organizational alignment. This position supports a pivotal role within

of Role The Enterprise Risk Management Director will play a critical role in driving a proactive and coordinated approach to risk management, helping the Company's long term growth by assessing and prioritizing risks and aligning management programs to mitigate risks that may impact the enterprise's ability to achieve strategic objectives. This role will support the develo

Manages all aspects of MRO spare parts inventory to support a pharmaceutical environment using a CMMS system (Maximo) and ERP system (SAP). This includes sourcing, ordering, receipt and stocking of all stock and non stock items. Key Responsibilities/Essential Functions Sources all required maintenance materials to support a pharmaceutical environment. Establishes supplier

of Role The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction of the manufacturing manager and on the floor guidance of the team lead, the manufacturing technician II will become qualified and independently capable

Lantheus is seeking an Azure Cloud Engineer to oversee and manage the Lantheus Managed Service Provider and collaborate with other engineers and stakeholders to deliver high quality cloud services. The ideal candidate will have a strong background in Azure Cloud services, infrastructure as code (IaC), and possess the ability to design, implement, and optimize cloud soluti

of Role Responsible for integrating and applying advanced knowledge of global regulations governing pharmaceutical drug development and commercialization to all aspects of assigned preclinical and/or clinical drug development programs, policies, and procedures, to ensure the rapid and successful development and registration of products while maintaining compliance with all

of Role Plans, organizes, directs and reports on quality activities to assure external partners and suppliers meet or exceed Lantheus' requirements for Pharmaceutical Products and Positron Emission Tomography (PET) Drug manufacturing. Key Responsibilities/Essential Functions Works closely with cross functional teams, including senior management levels, to ensure Lantheus m

of Role This role is responsible for leading Lantheus' Quality Systems & Compliance team. This role will oversee the global compliance function and related processes, providing multi site oversight of laboratory, manufacturing, and distribution operations. Manages and provides direction to Quality Systems, Compliance and Product Quality Complaints staff, ensuring that proc

The objective of this position is to lead a maintenance team and ensure effective and efficient coordination of all manufacturing maintenance and support activities. Specifically, this role will ensure manufacturing operations are supported, and any necessary corrective or preventive maintenance will include appropriate job plans, materials, manpower estimates, safety, ch

Lantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio. Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostic

of Role Perform routine and advanced testing on incoming materials, finished products and stability studies in QC Laboratory. Perform routine environmental monitoring and utilities testing. Area Specific Requirements Familiar with aseptic technique Perform Environmental Monitoring and utilities monitoring. Perform bioburden, sterility, endotoxin and other routine and advan

The objective of this position is to provide leadership and management oversight of cold (non radioactive) product manufacturing technical operations on the Billerica Campus, while ensuring compliance with all GMP, OSHA and other regulatory requirements. The Associate Director (AD) leads the manufacturing operations to deliver on time production of high quality pharmaceut