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Scientist (Virology, 1 Year Fixed-Term )

360biolabs is Australia's most comprehensive quality-accredited specialty laboratory services organisation. 360biolabs is a BioAgilytix company and part of a leading global contrac

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Bioagilytix Melbourne Source published Sep 20, 2026 Verified 7 hours ago
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Overview

360biolabs is Australia's most comprehensive quality-accredited specialty laboratory services organisation. 360biolabs is a BioAgilytix company and part of a leading global contrac

Full job description

360biolabs is Australia's most comprehensive quality-accredited specialty laboratory services organisation. 360biolabs is a BioAgilytix company and part of a leading global contract research organisation (CRO) supporting the development of innovative new medicines in a quality-controlled environment. At 360biolabs, we develop and conduct pharmacokinetics (PK) and pharmacodynamic (PD) assays across a wide variety of therapeutic areas to ensure the success of our clients' clinical trials and preclinical studies.

Working at 360biolabs means working with the best people (and technology) in our field. With a genuine focus on development, you will have access to local and global opportunities. You will also have access to a diverse offering of wellbeing and connection initiatives which reflects that people are our priority.

Provide scientific expertise and assistance in the development, validation, and conduct of virological assays for research, preclinical and clinical studies. To perform sample processing of virology assays to comply with relevant standards, regulatory guidelines and SOP requirements.

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.

General Laboratory Duties

Order and maintain supplies for the laboratories

Obtain quotes for relevant supplies

Ensure laboratory equipment is cleaned, maintained and calibrated as required

Ensure good housekeeping in the laboratory

Laboratory Assay Work

Assist in the development, optimization and validation of biological assays, particularly a range of virological and tissue culture techniques, including viral neutralisation assays and ELISA for use in human and animal trials supported by 360biolabs.

Perform assays for research projects, preclinical studies and clinical trials.

Data Analysis, Reporting and Document Work

Assist in the production of standard operating procedures

Maintain records to levels consistent with relevant standards and industry expectations

Perform data analysis, presentation and interpretation where appropriate

Assist in the production of both internal reports and reports for clients

NATA Accreditation

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.

Safety

Ensure the safe and efficient conduct of laboratory activities

Team Work

Maintain high levels of communication with colleagues

Professional Development

Attend meetings associated with clinical research or the work of 360biolabs

Participate in training activities and attendance at seminars in the field of expertise

Qualifications

BSc (Hon) in a Biological discipline plus relevant experience (Essential)

PhD in a Biological discipline OR equivalent experience (Desirable)

Experience / Knowledge / Attributes

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)

Strong background and proven experience in virological and tissue culture techniques and assays (Essential)

Experience in optimisation and validation of a range of virological assays including viral neutralisation assays and ELISA (Essential)

Experience in handling clinical samples and their analysis (Essential)

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)

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