About the Company
Cell Therapies Pty Ltd (CTPL) is an incorporated Australian Proprietary Company which manufactures and deploys advanced cell-based therapies to the global cell and gene therapy (CGT) market.
As a business, we are contracted by other companies to develop and manufacture their innovative products for Australian and international patients. In the last 15+ years, we have established our excellence in the field and are now acknowledged as an industry leader in delivery of these ground-breaking treatments to patients.
About the Role
We are seeking a motivated QC Analyst to support our facility and product manufacturing teams who manufacture clinical and commercial cellular therapy products in compliance with the Australian Code of Good Manufacturing Practice.
This Full-time position is 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.
We are recruiting for someone wanting to start their QC career within this exciting Biotech space through to a more senior Analyst with more than 5 years experience.
What an Analyst will be expected to do:
- Testing associated with cell therapy products including flow cytometry, qPCR, ddPCR, cell counting, cryopreservation, ELISA, and other cell based assays;
- Provide advice and recommendations to senior staff through research and analysis of various data sources
- Understanding equipment operation principles and maintenance;
- Adhering to standard operating procedures and Good Manufacturing Practice.
- Flexibility to planned operation task including weekends and overtime as necessary;
- Use of a variety of computer-based applications (MS Word, Excel, PowerPoint Outlook, BMS/EMS.
- For more experience candidates - establish new methodologies/techniques or assays as required within the QC group;
Skills & Experience
Essential:
- A Degree in a life sciences discipline or equivalent industry experience;
- High level of accuracy, technical capability and attention to detail;
- Ability to multitask and work autonomously as well as in teams:
- A diligent and quality-driven approach;
- A clear and confident communicator in a multidisciplinary team;
- Minimum 2-5 years experience in a Laboratory (Research, Pathology or GMP); and
- Experience in one of the following areas flow cytometry, qPCR, cell culture, cell based assay including ELISA;
Desirable:
- Experience in a GMP environment.
The Salary offered will be commensurate with skills, experience and industry standards. 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 close on 22 April.
Applications, including a CV and covering letter addressing the key requirements of the role, should be submitted via "Apply for this job" link below. Please note that only applications received through this link will be considered.