Analyst (PBMC)
Key Responsibility Areas
- The key responsibility areas (KRAs) are the major outputs for which the position is responsible and are not a comprehensive statement of the position activities.
- Order and keep accurate inventories of supplies for laboratory needs and forecast future needs based on projected project needs.
- Support the preparation of goods for assay work.
- Prepare worksheets.
- Ensure laboratory equipment is cleaned, maintained and calibrated as required
- Ensure good housekeeping in the laboratory
- Perform assays under supervision for research projects, preclinical studies, and clinical trials.
- Assist in the conduct of biological assays, particularly a range of immunology techniques and other assays.
- Support the performance of assays according to relevant Quality guidelines.
- Support the troubleshooting of assays.
- Maintain records (LIMS, database and paper) to levels consistent with relevant standards and industry expectations
- Support the preparation of summary tables.
- Adhere to ISO/IEC 17025, OECD Principles of GLP, GCLP Principles, 360biolabs' Quality Management System, and other requirements as per NATA Accreditation and regulatory guidelines.
- Ensure the safe and efficient conduct of laboratory activities
- Ensure compliance to relevant internal processes and statutory requirements
- Maintain high levels of communication with colleagues and productive relationships with service providers and other partners.
- Attend meetings associated with bioanalytical chemistry or the work of 360biolabs
- Participate in training activities and attendance at seminars in the field of expertise
Key Selection Criteria
- BSc in a Biological discipline (Essential)
- Honours or Masters in a Biological discipline or equivalent experience (Desirable)
Experience/ Knowledge/ Attirbutes
- Experience in medical laboratory techniques for the role required (Essential)
- Excellent organisational and writing skills (Essential)
- Ability to work as part of a team (Essential)
- Good communication skills (Essential)
- Experience in handling clinical samples and their analysis (Desirable)
- Experience with database computer software and file management (Desirable)
- Experience in the conduct of early phase clinical trials (Desirable)
- Experience in working in a quality-controlled environment preferably an accredited facility following ISO/IEC 17025, GLP or similar (Desirable)
- High motivation and enthusiasm for medical research and the progression of therapeutics and vaccines (Desirable)
Applications close on 22nd June 2026 at 9:15AM. For further information, please contact our Careers Team ([email protected]). Please submit your application via the job link if you're interested in joining us, as we're not able to process applications sent by email.
Apply now if you have what it takes to join our team!
360biolabs is a flexible, equal opportunity employer looking for committed and like-minded people to join us. Our culture is something we are very proud of, celebrating each individual and everything they bring to our team. We encourage applications from Aboriginal and Torres Strait Islander people, all members of the LGBTQIA+ community and people with a disability.
To express your interest in this position please submit a CV and cover letter. Applications only accepted from Australian / NZ residents with valid Australian work rights.
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