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Key skills for this role
Maintain awareness of International Standards and guidelines for Quality Systems
Conduct document control, including preparation, review and issue of new and updated documents; coordination of document reviews
Conduct internal audits
Investigate and report deviations and nonconformities; prepare and coordinate Corrective and Preventive Actions
Provide support to the Proficiency Testing Programme
Provide support to the equipment management programme, including equipment qualification and equipment calibration/service report review
Support staff training and competency programmes, including follow up of staff training records
Attend all required safety training and 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.
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.
Attend meetings associated with Quality Management or the work of 360biolabs
Participate in professional activities including attendance at conferences, training courses and seminars
Review policies, SOPs, systems and procedures to assure the quality and integrity of service offerings at 360biolabs
Quality assure client protocols and reports and conduct data integrity checks on data transfers
Maintain records (LIMS, database and paper) to levels consistent with relevant standards and industry expectations
Bachelor of Science (Hons) or equivalent qualification, plus relevant experience (Essential)
Two years' experience in Quality Assurance, working with Quality Management Systems (QMS), or equivalent relevant experience (Essential)
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Experience in a quality-controlled laboratory environment (preferably ISO/IEC 17025) (Essential)
Knowledge of laboratory techniques and assays (Desirable)
Excellent organisational and writing skills (Essential)
Ability to work as part of a team (Essential)
Good communication skills (Essential)
Proficient in use of Microsoft Office, including Word, Excel, and PowerPoint (Essential)
Experience with database software and file management (Essential)
Experience in the conduct of early phase clinical trials (Desirable)
High motivation and enthusiasm for medical research, therapeutic and vaccine development (Desirable)
Applications close on 23rd September 2026. 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. For further information, please contact our Careers Team (careers@360biolabs.com).
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.
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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.
#360biolabs
Parent group profile
BioAgilytix is a private global contract research organization providing bioanalytical testing for pharmaceutical and biotechnology companies.
Visit parent group websiteFull-time
Entry · 2+ years experience
Hybrid
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