CSL Seqirus influenza vaccine portfolio reaches millions of people every year, and every one of those products depends on labelling that is scientifically sound, regulatory compliant, and clear and informative for the end‑user. This role leads the function
CSL Seqirus in Stanford Dingley is looking for a Head of Global Labelling to shape strategic direction for labelling across their product portfolio. This leader will manage global teams and be responsible for the labelling approval process, ensuring
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, and
CSL Seqirus in Reading, England is seeking a Head of Pharmacovigilance and Regulatory Quality Assurance to lead and ensure compliance within their global quality function. This pivotal role involves managing the audit strategy, ensuring regulatory adherence, and guiding
PV Systems & Process Lead Patient safety depends on pharmacovigilance systems that work — and work well. In this role, youll be at the centre of keeping CSLs global PV system compliant, continuously improving, and inspection-ready across
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 —
Reporting to the Site Head of Quality Assurance, the Head of Front Line QA (and QP, if eligible) provides independent QA/QP oversight for all operations at Seqirus Liverpool, as well as support to commercial affiliates and contract
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,
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
Quality in clinical development is a matter of operational resilience as much as regulatory mandate. This role serves as a CQA Auditor within our Research & Development Quality audit program, responsible for executing the global audit
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