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
The role of the Enterprise Manager, EMEA Trade Compliance is responsible for the execution and maintenance of CSL’s world-class import-export compliance program in the EMEA Region. Its focus is to ensure all CSL legal entities operating in EMEA
Every adverse event report that reaches CSL — from a treating physician, a license partner, a regulatory authority — starts its life in one place: intake. This role owns the quality of that starting point. Youll oversee
Responsibilities: Under general direction, provides support on Quality systems to ensure compliance with company standards and GMP regulatory guidelines Develops, maintains and improves GMP-related quality control systems including standard operating procedures (SOPs) Participates in project teams
The role is part of the Accounting Operations, Account to Report team within the Centre of Excellence. The Senior Reporting Accountant is responsible for the execution and coordination of defined accounting and close activities for a
This position is to backfill an existing role which was vacated through internal promotion. The role is part of the Account to Report team and is responsible for Financial Accounting for one or more entities to
Principal Clinical Scientist (Senior Clinical Scientist level also considered) The Role Were looking for a clinical scientist — someone who has been the scientific lead for clinical studies before, from protocol development to start-up (development of
Job Description The Opportunity A rare and exciting opportunity has arisen to join our well established Global Seqirus legal team as the Legal Counsel, EMEA. Reporting through to the Seqirus Associate General Counsel, EMEA you will
GLP Vendor Oversight and QA Lead The integrity of nonclinical data depends on more than what happens inside a companys walls. Much of the critical work in GLP-regulated research — safety studies, toxicology, analytical testing —
Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission
Responsibilities: • Responsible for leading process improvement activities and staff in support of CSL and industry best practices • Defines improvement projects aligned with business strategies • Establishes and implements processes supporting global standardization and reporting strategies
Responsibilities: • Under limited supervision, provides technical support for validation and maintenance of production equipment, utilities and systems• Monitors quality and system standards to ensure reliability and compliance with company standards and governmental regulatory requirements• Verifies
Who Are CSL? We are a leading international critical IoT connectivity expert provider specialising in sectors including Building & Security, Healthcare & Telecare, Infrastructure, Retail & Hospitality, and Transport & Logistics. We are a rapidly growing, private
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
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
Job Description Company description CSL Seqirus is part of CSL. Ready to make your application Please do read through the description at least once before clicking on Apply. As one of the largest influenza vaccine providers in the
Job Description CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means
Job Description 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
The Manager, HR Service Center is responsible for leading and developing a team of five HR Operations Advisers to deliver high-quality, compliant, and customer-focused HR services across 23+ countries in EMEA. The role drives operational excellence
Every adverse event report that reaches CSL from a treating physician, a license partner, a regulatory authority starts its life in one place: intake. This role owns the quality of that starting point.Youlloversee the vendor responsible for