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Form of workAbout the company:
Magellan Stem Cells is undertaking Phase III clinical trials in collaboration with our clinical partners and universities and is committed to bringing cellular therapy to patients in need with ethical, professional and the highest safety standard of care. Newly completed state of the art cleanroom manufacturing and laboratory facilities will enable Magellan to manufacture and test cell therapy treatment to GMP/GLP standards.
The role:
A new exciting opportunity has arisen for a suitably qualified stem cell Quality Control Analyst, to work in a busy laboratory within a close-knit professional team.
Reporting to the Quality Manager, you will be responsible for performing laboratory activities that includes routine and research work in cell culture using aseptic techniques and following Standard Operating Procedures (SOPs). Testing includes Elisa Immunoassays, Cell Counting, Trilineage Differentiation and Raw Material testing. You will work in a laboratory cleanroom environment with strict adherence to laboratory procedures and follow a GMP/GLP quality management system to carry out various tests related to stem cell culture product Quality Control. Responsibilities will also include test method development, troubleshooting and maintaining Magellan’s compliance with current regulatory requirements.
This position will liaise with subcontract testing laboratories that perform specialised testing including microbiological testing. Other related areas of involvement include safety, inventory management, and support for facility technical instrumentation and services. This full-time role will suit a reliable individual with initiative and ownership for delivering outcomes.
