The Company

Starting a century ago, CSL made a promise to save lives and protect the health of people stricken with a range of serious and chronic medical conditions. Today that same promise has never been stronger.

With operations in more than 30 nations and over 14,000 employees worldwide, we develop and deliver biotherapies to prevent and treat people with life-threatening medical conditions. Our broad-range of therapies include those to treat disorders such as haemophilia and primary immune deficiencies, and vaccines to prevent influenza.

We collaborate with patient and biomedical communities to improve access to therapies, advance scientific knowledge, and support future medical research. Our world-class commercial operation, combined with a large and focused R&D team and operational excellence, enable us to accurately identify, successfully develop, and dependably deliver innovations that patients and providers want.

For a century, CSL has earned a reputation as a passionate yet responsible organization, driven to care for patients and deliver on its commitments.

The Opportunity

This is an opportunity to join the Bioanalytical department on a 12m contract, working alongside other scientists you will support GMP assay and equipment qualification and technology transfer to support the development of recombinant proteins and other biopharmaceuticals.

This role will be based at our Parkville office with some work required at our new, state of the art building at 645 Elizabeth Street, North Melbourne.

Duties Include:

• Perform routine assays in support of process development activities
• Maintain laboratory quality systems and records of analytical results
• Actively contribute to technical discussions
• Transfer assays from / to global sites
• Write qualification plans, experimental data packages, analytical documents and reports
• Contribute to change controls and deviations
• Support equipment and software qualification / validation

To be successful

• Tertiary Qualification in relevant field (Chemistry, Biochemistry, Pharmaceutical)
• Understanding of operational and quality requirements for qualification and transfer of methods for early phase clinical trials
• Experience in (U)HPLC, capillary electrophoresis and / or plate based assays
• Experience working in a GMP environment
• Experience of electronic systems within an analytical laboratory (ELN, instrument software)
• Experience of electronic quality systems (LIMS)
• Motivated individual with a strong commitment to quality and time management
• Proactive, well organized and have strong interpersonal skills

Applications close 5pm AEST 7th April 2023.

Employment screening, including criminal history, medical assessment, confirmation of experience and stated qualifications, Australian working rights and other relevant checks form part of the candidate suitability evaluation process.

Our Benefits

We encourage you to make your well-being a priority. It's important and so are you. Learn more about how we care at CSL.

About CSL

CSL is a leading global biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL .

We want CSL to reflect the world around us

As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

Do work that matters at CSL!