Pharmaceutical jobs in Australia

Entity: CSL Behring

Job Category: Quality

Job Family: Quality Control

Job Type: Full Time

Location: Broadmeadows, Victoria, Australia

Employer Reference: R-283589

The Company

CSL Limited is a company that fosters a work culture emphasising Superior Performance, Innovation, Integrity, Collaboration and Customer Focus with a commitment to support, train and grow its people. As a genuine leader in the biopharmaceutical industry, CSL is a multinational ASX Listed Company that is actively growing its Australian based manufacturing operations to support global growth. CSL develops, manufactures and markets products to treat and prevent serious human medical conditions and is globally one of the largest manufacturers of plasma-derived therapies.

The Opportunity:

Join CSL Behring at our Broadmeadows site as part of the QC Sample Management team, where we currently have three exciting opportunities available.

In this role, you will play a key part in the efficient coordination and management of samples supporting Biochemistry, Microbiology, and Chemistry testing. You will help ensure all activities are performed safely, efficiently, and in compliance with GMP requirements, approved test methods, and laboratory standards.

As part of a site undergoing significant expansion and investment, you will contribute to the growth of world-class manufacturing capabilities that support Australia’s export economy, create highly skilled employment opportunities, and enable the local development and commercialisation of next-generation medicines.

CSL Behring (Broadmeadows) is undergoing extensive and positive change as we expand our capability and capacity. In addition to contributing to Australia’s export economy, CSL has invested in substantial new manufacturing facilities at Broadmeadows that will provide Australia with further high skills science and manufacturing employment opportunities and strengthen capabilities to develop and commercialise future new medicines onshore in Australia.

The Role

• Ensure compliance with the Code of Responsible Business Practice, Global Quality Policy, Site Quality Manual, and applicable cGMP requirements in all laboratory activities.
• Perform laboratory duties, including routine QC testing, assay execution, and support of day-to-day laboratory operations.
• Manage laboratory housekeeping, inventory, stocktakes, ordering of materials and reagents, and monitoring of in-house standards and controls to meet QC testing requirements.
• Maintain and calibrate laboratory equipment and facilities in accordance with approved procedures, and troubleshoot equipment malfunctions as required.
• Complete, review, verify, enter, file, and archive laboratory records and test data, including LIMS entries, batch records, and GMP documentation.
• Coordinate QC sample management activities, including sample distribution within QC, external testing, and associated record management.
• Support the preparation, review, and updating of procedures, forms, and test methods through approved systems, while contributing to continuous improvement initiatives using Lean Six Sigma principles.

To be successful

• Tertiary qualification in a relevant scientific discipline.
• Ability to follow laboratory test procedures, operate laboratory equipment, and work effectively within a LEAN laboratory environment.
• Knowledge and practical experience of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Windows-based software applications.
• Strong organisational, time management, and problem-solving skills, with the ability to ensure testing and activities are completed within required timelines.
• High attention to detail and commitment to the accurate, thorough, and compliant completion of laboratory activities.