We are seeking a detail-oriented QC Biochemist to join our Quality Control team.
Reporting to the QC Team Leader, you will be responsible for executing routine laboratory testing and supporting activities in line with Good Manufacturing Practice (GMP), ensuring quality, safety, and compliance standards are consistently met.
This is an exciting opportunity to contribute to a high-performing laboratory environment while supporting the delivery of critical quality outcomes.
This role will be based in Broadmeadows.
Key Responsibilities
Perform routine analytical testing in line with approved procedures and schedules
Accurately record, review, and enter results into LIMS
Manage samples, including logging, tracking, and distribution
Ensure compliance with GMP, GDP, and quality standards
Identify and escalate OOS results, deviations, and quality issues
Maintain laboratory documentation, records, and SOPs
Support equipment maintenance, calibration, and troubleshooting
Manage lab stock, reagents, and consumables
Follow safety procedures and report hazards/incidents
Contribute to continuous improvement and validation activities
Collaborate with internal teams and support training as required
Your Experience
Tertiary qualification in a relevant scientific discipline (e.g. Chemistry, Microbiology, Biochemistry)
Experience in a pharmaceutical or GMP-regulated QC laboratory
Strong knowledge of GMP and/or GLP
Experience with ELISA testing and Flow cytometry preferable
Experience with laboratory instrumentation and analytical testing such as manual and electronic pipettes
Strong attention to detail and documentation skills
Ability to work independently and manage time effectively
Solid communication and teamwork capabilities
Proficiency in Windows-based systems (LIMS experience preferred)
Why Join Us?
Opportunity to work in a regulated, high-impact manufacturing environment
Be part of a collaborative and supportive QC team
Contribute to continuous improvement and innovation initiatives
Develop your technical and compliance expertise
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/
Our Benefits
For more information on CSL benefits visit How CSL Supports Your Well-being | CSL
You Belong at CSL
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging
Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement
