Scientist (Molecular)

Posted 7 Days Ago
Be an Early Applicant
Melbourne, Victoria, AUS
In-Office
Mid level
Biotech
The Role
Develop, validate and run molecular assays (RNA/DNA extraction, qPCR, dPCR, NGS) for research, preclinical and clinical studies. Process clinical samples, maintain lab equipment, ensure compliance with ISO/GLP standards, perform data analysis and produce SOPs and reports.
Summary Generated by Built In
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 molecular assays for research, preclinical and clinical studies. To perform sample processing of molecular assays to comply with relevant standards, regulatory guidelines and SOP requirements.

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.
    • 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 molecular biology techniques, including RNA/DNA extractions, dPCR, qPCR, genotyping and Next Generation Sequencing 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
          • 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

Key Selection Criteria

  • 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 molecular biology and NGS  techniques (Essential)
  • Experience in optimisation and validation of a range of molecular assays including qPCR, dPCR and Next Gen Sequencing. (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)

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.

 

#360biolabs

Skills Required

  • BSc (Hon) in a Biological discipline plus relevant experience
  • PhD in a Biological discipline OR equivalent experience
  • Experience in medical laboratory techniques
  • Excellent organisational and writing skills
  • Ability to work as part of a team
  • Good communication skills
  • Strong background and proven experience in molecular biology and NGS techniques
  • Experience in optimisation and validation of molecular assays including qPCR, dPCR and NGS
  • Experience in handling clinical samples and their analysis
  • Experience with database computer software and file management
  • Experience in the conduct of early phase clinical trials
  • Experience working in a quality-controlled accredited facility (ISO/IEC 17025, GLP or similar)
  • High motivation and enthusiasm for medical research and therapeutics/vaccines
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The Company
HQ: Durham, NC
841 Employees
Year Founded: 2008

What We Do

BioAgilytix is a leading global contract research organization focused on supporting pharmaceutical and biotech partners in all phases of drug development. With laboratory locations in North Carolina’s Research Triangle Park; Cambridge, Massachusetts; San Diego, California; Melbourne and Brisbane, Australia and Hamburg, Germany, BioAgilytix provides PK, immunogenicity, biomarkers, and cell-based assay services supporting the development and release testing of therapeutics across a number of industries and disease states. BioAgilytix offers assay development, validation, and sample analysis under non-GLP, GLP, and GCP, as well as GMP quality control testing (i.e., product release testing, stability testing, etc.) BioAgilytix also offers diagnostic testing services at its CLIA-certified, CAP-accredited Boston laboratory. BioAgilytix’s team of highly experienced scientific and QA professionals ensures high-quality science, data integrity and regulatory compliance through all phases of clinical development. BioAgilytix is a trusted partner to many top global pharmaceutical and biotech companies. For more information, visit www.bioagilytix.com.

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