Manufacturing Scientist

About the Company Cell Therapies Pty Ltd (CTPL) is a commercial Contract Development and Manufacturing Organisation (CDMO) located within the Peter MacCallum Cancer Centre. We specialise in the development and delivery of cell and gene therapies and have more than 20 years’ experience in this area. The growth of CTPL will continue through our commitment to supporting both Australian and international research and development activities, alongside delivery of commercial contracts to provide these highly personalised therapies to patients in Australia and the region.

About the Role

We are seeking a motivated Manufacturing Scientist to join our growing team. As a Manufacturing Scientist, you will be tasked to perform critical aseptic manufacturing processes involving cell culture of CAR-T Cells and others for clinical and commercial cellular therapy products. These products must comply with the Australian Code of Good Manufacturing Practice (GMP) for human blood and blood components, human tissues and human cellular therapy products. This is a Full-time position located at our new, state-of-the-art Melbourne facility, located at the Peter MacCallum Cancer Centre on the edge of the CBD in Australia’s most dynamic biomedical precinct. This is a great opportunity to gain experience and get directly involved in the newest advanced therapies that can make a serious impact on patient’s lives.

Duties

1. Aseptically manipulating and processing human cells, tissues and blood components in a Grade B cleanroom environment using manual and automated cell culture techniques in compliance with GMP guidelines;
2. Set up manufacturing kits, cleanrooms and equipment for manufacturing processes;
3. Performing in-process environmental monitoring and contamination risk-mitigation;
4. Adhering to standard operating procedures and Good Manufacturing Practice (GMP);
5. Completing batch records and other facility documentation;
6. Performing calibration and preventative maintenance activities related to process equipment;
7. Participating in manufacturing process improvement activities and document preparation;
8. Routine overtime and some weekend work will be required and paid at overtime/penalty rates in excess of the base salary;
9. Use of a variety of computer-based applications.

Skills & Experience

1. A degree in a life sciences discipline or equivalent industry experience;
2. At least 2-3 years experience with the manipulation of human cells, tissues, plasma and/or blood components;
3. Experience working within a cleanroom environment and working in biosafety cabinets;
4. GMP experience essential;
5. Experience working in cell culture including aseptic media preparation, cell culture inoculation and harvests, performance of cell viability and cell counts, use of microscopes, performing calculations, pipetting, performing dilutions and aliquoting;
6. Experience with large scale cell culture equipment such as cell savers, bioreactors, filtration systems would be advantageous;
7. High level of accuracy, technical capability and attention to detail;
8. A diligent and quality-driven approach;
9. A clear and confident communicator;
10. Ability to multitask and work autonomously as well as in teams;
11. Comfortable working within a hospital environment.

The salary offered will be commensurate with skills, experience and industry standards. The team currently works a 4 day week – Monday to Thursday or Tuesday to Friday. Company specific GMP training will be provided as part of the induction process. If you think you have what it takes to be part of a dynamic team for a company that is in a very exciting growth phase, then APPLY NOW! Applications should include a CV and a covering letter addressing the key requirements of the role. Please note that only applications received via SEEK will be considered. The selection process will include a practical skills assessment task. Application closes on 21 February 2025.

Right to live and work

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