Jobs at CSL

Lead global plasma procurement strategy and team to secure supply continuity, reduce total cost of ownership, manage supplier risk/compliance, and drive innovation across equipment, consumables, technology, facilities, and services. Partner with senior Plasma and enterprise stakeholders, own category KPIs, and sponsor cross-functional transformation to improve procurement maturity in a regulated environment.

Plan and manage clinical trial supplies for low-to-medium complexity studies: forecast drug volumes, collect/analyze samples, ensure storage/transport/archiving, manage vendors, use IRT, author/review study documents, lead global CTS meetings, partner with R&D, and update SOPs for continuous improvement and compliance.

Lead local regulatory activities in Turkey: supervise Local Regulatory Support, manage Health Authority engagements, ensure compliance and readiness for inspections, prepare local submissions (Module 1), support labeling and promotional review, coordinate cross-functional regulatory strategies for product registrations and lifecycle management, and represent the company with industry groups and stakeholders.

Lead regional regulatory strategy and health authority interactions for assigned products, support preparation of regulatory submissions and Module 1 documentation, contribute to global regulatory strategy (GRAST), maintain regional regulatory knowledge and stakeholder communications, update regulatory systems (e.g., Veeva), and drive timely, positive regulatory outcomes in a hybrid US location.

Lead global analytical strategy for biopharmaceutical development, oversee analytical method development/validation (LC-MS/MS, ligand binding, biomarkers, immunogenicity), ensure regulatory compliance and inspection readiness, support regulatory submissions, troubleshoot technical challenges, and manage teams, CROs and analytical infrastructure.

Lead Americas learning strategy and deliver leadership, managerial, and employee development programs. Partner with HR and business leaders to design, implement, measure, and improve digital and in-person learning, onboarding, mentoring, assessments, and succession planning. Manage vendors, budgets, and an Americas L&D team; facilitate programs and ensure alignment with enterprise talent strategies, inclusion goals, and regulatory requirements. Support career and development planning and leadership assessments to drive retention and talent mobility.

Lead month-end close and statutory reporting for the Colombian entity, ensuring IFRS and local compliance. Manage reconciliations, audit coordination, internal controls, ERP interfaces, and process improvements while supporting tax, AP, treasury, and balance sheet planning.

Lead translational and preclinical immunology research to support therapeutic portfolio: design and run in vitro/ex vivo studies, develop PD/biomarker strategies and assays for toxicology and early clinical studies, collaborate with in vivo pharmacology, clinical development, CROs, and cross-functional teams, contribute to regulatory and clinical documents, and shape research strategy and external scientific networks.

Lead and manage day-to-day and strategic research laboratory operations for Waltham and Schlieren, overseeing vendors, IFM contracts, capital budgets, compliance, cross-functional teams, and continuous improvement to enable safe, efficient, and standardized scientific research.

Lead enterprise value realization for I&T investments: shape business cases, track and forecast benefits, govern portfolio value delivery, report to executives, and partner with Finance and stakeholders to optimize ROI.

Senior commercial finance business partner supporting international and pandemic portfolios (~$1bn revenue). Provide FP&A, strategic financial leadership, complex modelling, business-case review, audit support, internal controls, and lead a finance team to guide pricing, launches, resource allocation, and commercial strategy.

Perform collections and cash application tasks: run aging reports, resolve payment and remittance issues, liaise with collection agencies and internal teams, process write-offs and credits, respond to customer queries, and support continuous improvement projects to boost customer satisfaction.

Lead and govern laboratory compliance across CSL Melbourne research labs and vivarium. Develop compliance frameworks, manage audits/inspections, oversee CAPAs/deviations/change controls and risk registers, govern training and documentation, and partner with QA, EHS, Facilities and research teams to ensure regulatory readiness and continuous improvement.

The Associate Director, Federal Government Affairs will manage strategies for CSL Behring's federal interests, engage with stakeholders, provide policy insights, and collaborate on advocacy efforts.

Lead epidemiology strategy and programs for assigned products, design and execute studies, manage data and vendors, contribute to regulatory submissions, drive RWE use, perform benefit-risk assessments, and support departmental process improvement and cross-functional leadership.

Lead global workplace strategy, standards, and program development. Oversee space planning, moves, renovations, and project delivery; manage regional teams and external partners; drive change management, sustainability, analytics, governance, and reporting to optimize employee experience and costs.

Lead site supply chain for a vaccine manufacturing site: plan capacity and campaigns, manage inventory and warehouse operations, own product supply strategies, ensure SAP data integrity, drive S&OP and pandemic readiness, partner with global functions (procurement, quality, logistics), and lead a ~30-person team to meet financial, quality and regulatory targets.

Coordinate and support outsourced nonclinical studies: manage contracts, POs and SAP entries, maintain documentation and trackers, schedule global meetings, liaise with vendors (German C1), support vendor qualification and third-party risk, and improve digital workflows using SharePoint, Excel dashboards and Power BI.

Lead and coordinate project and portfolio activities across R&D, design integrated processes for product development and manufacturing transfer, support technology platforms, monitor project progress and compliance, and contribute to lifecycle planning and risk management under supervision.

Lead finance business partnering for Clinical Operations within R&D. Build relationships with clinical leadership, own financial planning, forecasting, reporting, and governance. Drive advanced financial modeling, portfolio investment decisions, study-level budgeting, due diligence for collaborations/acquisitions, and transformation of finance processes. Manage and develop a team of finance professionals and deliver executive-ready insights to influence strategic decisions.