This role has responsibility to ensure supply plans are met by driving batch release activities and specific Contract Manufacturing Organisations (CMO) activities across multiple products and markets. The role also ensures up to date status and
The Senior Financial Analyst supports global accounting operations by delivering accurate financial analysis, reconciliations, and close and planning cycle support. This role helps maintain reliable financial data, with emphasis on intragroup profit elimination and transactional FX
The role is part of the Accounting Services Team and will be responsible for managing the monthly and close global operations activities in line with Global processes and policies Responsibilities Lead a close operations team in
CSL is seeking a highly organized and proactive Regional Total Reward Analyst to support the Regional Sr. Manager – EMEA. The individual must be fluent in English and German. This role supports EMEA Total Reward programs across
Quality in clinical development is a matter of operational resilience as much as regulatory mandate. This role serves as a GCP Auditor within our Research & Development Quality audit program, responsible for executing the global audit
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
Responsibilities: • Under limited supervision, provides production support, setting up production procedures and labels • Operates manufacturing equipment following standard procedures and current Good Manufacturing Practice (cGMP) • Tracks equipment performance and adjusts setups, calibrations and
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
Under limited supervision provides comprehensive daily administration support to the Liverpool site with some specific duties aligned to provide support to EHS. Undertaking other ad hoc duties as required within the Liverpool site. RESPONSIBILITIES Support for
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 be responsible
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
Responsibilities: • Under direct supervision, assists with the setup and operation of production equipment • Operates manufacturing equipment following standard procedures and current Good Manufacturing Practice (cGMP) • Determines and corrects minor machine malfunctions • Enters
Responsibilities: • Under limited supervision, provides production support, setting up production procedures and labels • Operates manufacturing equipment following standard procedures and current Good Manufacturing Practice (cGMP) • Tracks equipment performance and adjusts setups, calibrations and
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. 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
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
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
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
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