Quality in a globalized drug safety network is a matter of operational resilience as much as regulatory mandate. This role serves as a GVP Auditor within our Research & Development Quality audit program, responsible for executing
CSL R&D is driving significant transformation accelerating its data and AI ambitions in a way that demands architecture thinking rooted in business value, not just technical delivery. The R&D Data Architect is a brand new role, created
Head of Global Labelling Hiring Immediately
Head of Global Labelling The Role CSL Seqirus influenza vaccine portfolio reaches millions of people every year, and every one of those products depends on labelling thats scientifically sound, regulatory compliant, and is clear and informative for
Director, Regional Ecosystem Lead (Northern Europe & UK) Hiring Immediately
CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part
The Manager, Global Labelling Operations (GLO) is part of a team of labelling professionals responsible for managing and executing the technical and operational elements that support the development, review and approval of product packaging components globally,
The Director, Regulatory Platforms holds strategic oversight and operational accountability for the technology systems that power CSLs Global Regulatory Affairs and Safety organisation including Regulatory Information Management, Submissions Management, Submissions Archive, Publishing, Labelling, Regulatory Intelligence, and Collaboration.
Responsible for shaping the future capabilities, governance framework, and sustainability agenda of Global Procurement. The role partners with the CPO, Procurement Leadership Team, HR, and business stakeholders to strengthen procurement maturity, enable organizational effectiveness, develop future
The role of the Head of Global Logistics is to p rovide enterprise leadership and accountability for the execution of Seqirus global logistics strategy, ensuring the secure, compliant, and cost-effective flow of raw materials, intermediates, finished
The Head of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs,
The role of the Head of Global Logistics is to provide enterprise leadership and accountability for the execution of Seqirus’ global logistics strategy, ensuring the secure, compliant, and cost-effective flow of raw materials, intermediates, finished goods,
Seqirus seeks a Head of Global Logistics to lead the enterprise logistics strategy and execution across a regulated, global manufacturing network. The role drives service reliability, compliance, cost optimization, and resilience through global teams and strategic
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables
The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides
Position Overview: The HRBP is a key member of the Human Resources function, supporting the delivery of HR initiatives that drive business results and foster a values-based culture. Reporting into the Senior Director/Director HR Business Partner,
Company description CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With
CSLs R&D organization is accelerating innovation to deliver greater impact for patients. Find out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now. With a project-led structure and a
The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides
Head of Global Labelling The Role CSL Seqirus influenza vaccine portfolio reaches millions of people every year, and every one of those products depends on labelling thats scientifically sound, regulatory compliant, and is clear and informative for