With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.
CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL’s therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.
We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!
To lead a shift team for Inspection and Packing (I&P) operations to achieve the production schedule to agreed standards of People Development and support, cGMP, HSE, Productivity and Cost.
Responsible for adherence to standards across all activities including reporting and resolution of issues.
Participation in site wide management activities, projects and improvements.
Expected to operate in or support alternative production areas of Liverpool Site Manufacturing when required.
Develops and maintains training plans and agility matrices to support cross functional working
Manages activities in assigned area to assure timely production in accordance with company policies and regulations
leads investigations in HSE and Quality. Supports investigations in adjacent areas as required.
Develops and implements manufacturing schedules and procedures, allocates labor and capital resources to maximize productivity
Plans and manages production line downtimes to minimize disruptions to manufacturing schedules
Ensures the effective use of materials, equipment and employees in producing quality products
Formulates and recommends manufacturing policies, procedures and programs
Leads & champions changes, innovations and improvements. Participates in I&P project teams
Runs and supports cross functional meeting processes as required.
Leads and supports process improvements
Ensures budgets, schedules and performance requirements are met
Manages KPI data management and reporting
Deputise for Process lead as required at accountability boards, monthly meetings.
Bachelor degree, or equivalent in related field, or equivalent vocational or technical education
5 or more years' manufacturing experience in inspection and/or packing processes
1–3 years’ experience of managing a shift team in a pharmaceutical, biotechnology, biological or highly regulated industry
Experience of developing a positive HSE behavioural culture on a shift operation
Experience of leading and implementing improvement activities
Experience of the use and application of lean continuous improvement tools and techniques