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Conduct filter integrity testing and environmental monitoring.
Ensure compliance with Good Manufacturing Practices (GMP) and CSL's quality policies.
Complete batch documentation accurately and timely.
Support process development, innovation, and troubleshooting within the manufacturing plant.
Maintain a clean and orderly manufacturing facility.
Liaise with cross-functional teams to meet customer requirements.
Your Skills and Experience
Experience in the pharmaceutical or allied industry.
Technical skills in manufacturing and quality processes.
Knowledge of cGMP and plasma fractionation.
Strong communication and relationship skills.
Proficiency in Microsoft Office applications.
Preferred tertiary qualification in science/engineering or relevant experience (minimum of VCE qualification).
Why CSL Behring?
Be part of a global leader in biopharmaceuticals.
Work in a collaborative and innovative environment.
Opportunities for professional growth and development.
Competitive salary and benefits package.
How to Apply
If you are passionate about making a difference and want to be part of a dynamic team, please submit your application including your CV in one document.
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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 Behring
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.
Do work that matters at CSL Behring!