About CSL
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!
Job Description
The Opportunity
An exciting opportunity has become available within the Biotechnology Manufacturing Facility at our Broadmeadows site. We are seeking a Manufacturing Technician to provide formulated cGxP compliant inputs to the manufacturing operations.
The CSL Biotechnology Manufacturing Facility is part of the CSL R&D Group. In this facility we use mammalian cells and DNA technology to manufacture drugs that will be used to treat life-threatening diseases.
We work in collaboration with Process Development, Quality, and other technical and business functions in order to ensure efficient and safe drug substance manufacturing processes for the production of multiple recombinant proteins.
The role
Reporting to the Senior Manufacturing Manager Upstream Operations, your responsibilities will include:
Ensure compliance with applicable cGxP regulations
Weighing and dispensing of reagents
Equipment and environmental cleaning
Operation of mixers for process solution preparation
Utilise relevant ERP and business systems (PMCS, MES, StarLIMS, Historian) to control and document raw material and process related functions
Ensure that all deviations are reported; where appropriate support the investigation into the deviation
Under the guidance of relevant Manufacturing Assistant, Associate or Supervisors review and revise forms, procedures, batch records and other operational related documentation
To be successful
Minimum of VCE qualification and/or related industry experience
Some manufacturing experience is preferred
Ability to work independently and as part of a team
Strong written and verbal communication
Demonstrated problem solving skills
Flexibility and adaptability to work across multiple manufacturing areas
Apply now to utilise your technical background in a modern and world class recombinant facility!
Applications close 5pm AEST on the 18th of June 2021.
Applications must address the selection criteria above and include a current CV and covering letter.
