About this course
This course provides a practical introduction to working in cleanroom environments used in GMP biopharmaceutical manufacturing.
Participants will learn the principles of contamination control, gowning, and aseptic technique, and gain hands-on experience performing environmental monitoring on industry-aligned equipment.
The course also introduces environmental monitoring concepts and how monitoring data is used to maintain cleanroom standards, identify potential risks, and support deviation investigations and corrective and preventive actions (CAPA) in GMP settings.
Learning outcomes
- Demonstrate correct gowning and entry procedures for cleanroom environments
- Apply aseptic technique when working in a biosafety cabinet
- Understand key principles of contamination control
- Describe how environmental monitoring supports GMP compliance
- Recognise risks that may impact cleanroom integrity and understand how deviations and CAPA support contamination control and GMP compliance.
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schedule 1 day
3 hours self-paced online learning. 3.5 hours in-person training.
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book_ribbon Blended learning
Build fundamentals online, apply in person.
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location_on BIF
In person training delivered at the BIF.
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help On request
Please contact us for pricing.
Target audience
This course is suitable for:
- Students preparing to enter biopharmaceutical manufacturing
- Early-career professionals seeking GMP cleanroom experience
- Researchers transitioning into bioprocessing environments
- industry staff requiring refresher training in aseptic technique
Assessment and outcomes
Participants will complete a short online quiz following the course to reinforce key concepts.
Upon successful completion, participants will receive a certificate of completion and digital badge
Discuss your training needs
Contact us about enrolling in a course or we can run a tailored course for your team. Email: bif@uts.edu.au