Join an exciting, rapidly growing company at the forefront of cell and gene therapies. Cell Therapies Pty Ltd (CTPL), a commercial Contract Development and Manufacturing Organisation (CDMO) located within the Peter MacCallum Cancer Centre, is looking for a motivated and skilled Manufacturing Scientist to contribute to the development of life-changing therapies.
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About the Company
CTPL specializes in the development and delivery of cell and gene therapies. With over 20 years of experience, we are committed to supporting Australian and international research and development activities, along with delivering commercial contracts for highly personalized therapies for patients in Australia and the region.
About the Role
We are seeking a Manufacturing Scientist to join our dynamic team at our state-of-the-art Melbourne facility. In this full-time position, you will be responsible for performing critical aseptic manufacturing processes involving the cell culture of CAR-T Cells and other therapeutic products for clinical and commercial applications. You will work in a cleanroom environment under the Australian Code of Good Manufacturing Practice (GMP) for human blood components, tissues, and cellular therapy products.
Key Duties & Responsibilities:
- Perform aseptic manipulation and processing of human cells, tissues, and blood components in a Grade B cleanroom environment using manual and automated cell culture techniques in compliance with GMP guidelines.
- Set up manufacturing kits, cleanrooms, and equipment for manufacturing processes.
- Conduct in-process environmental monitoring and contamination risk mitigation.
- Adhere to standard operating procedures and GMP.
- Complete batch records and facility documentation.
- Perform calibration and preventative maintenance activities related to process equipment.
- Participate in manufacturing process improvement activities and document preparation.
- Work overtime and on weekends as required (paid at overtime/penalty rates).
- Use various computer-based applications.
Skills & Experience Required:
- Degree in life sciences or equivalent industry experience.
- At least 2-3 years of experience manipulating human cells, tissues, plasma, and/or blood components.
- Experience working within a Grade B and C cleanroom environment, and using biosafety cabinets.
- Essential GMP experience.
- Strong aseptic techniques, with experience in open manipulations, culture bags, and flask work within a biosafety cabinet.
- Experience with large-scale cell culture equipment such as Prodigy, Cocoon, or bioreactors is advantageous.
- High accuracy, attention to detail, and technical capability.
- A diligent, quality-driven approach.
- Clear and confident communication skills.
- Ability to multitask, work autonomously, and within teams.
- Comfort working in a hospital environment.
Benefits & Salary:
- Salary commensurate with skills, experience, and industry standards.
- Company-specific GMP training provided during induction.
- Team works a 4-day week (Monday to Thursday or Tuesday to Friday).
How to Apply:
If you are ready to be part of an innovative company in a growth phase, APPLY NOW! Applications should include a CV and cover letter addressing the key requirements of the role. Please note that only applications received via SEEK will be considered.
For more information, visit our website: www.celltherapies.com