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Quality Control Analytical Technology Scientist

Job description

Benefits
  • Work with one of the world’s most respected biopharma organisations
  • Join a high-calibre scientific team working on impactful therapeutic products
  • Gain exposure to innovative immunoassay and biochemistry techniques
  • Standard Monday to Friday hours 
  • Collaborative team of specialists and career-enhancing experience in GMP
About the company
Work within a large global Biotechnology company that boasts a good company culture that is always expanding.

About the opportunity
This 12-month contract role sits within the Quality Control Analytical Technologies team, supporting analytical activities related to method development, validation, and transfer. Based in a biochemistry-focused lab environment, you’ll play a critical role in the scientific and regulatory support of biological product testing, reporting to the Head of QCAT. This is a fantastic opportunity for a QC Scientist or Analyst with biochemistry or molecular biology experience to take on a project-based scientific role within a supportive and quality-driven team.


Resposibilities:
  • Develop, validate, and transfer analytical methods for biological products
  • Design and execute experimental plans in accordance with project objectives
  • Prepare and review scientific documentation including SOPs, protocols, and validation reports
  • Perform analytical testing using immunoassay-based techniques (e.g., ELISA, nephelometry)
  • Ensure accuracy and data integrity in accordance with GMP and regulatory standards
  • Participate in project meetings and regulatory discussions
  • Coordinate timelines and schedules for yourself and supporting analysts
  • Provide insights and support for process improvements, investigations, and quality submissions

Must have
  • Bachelor’s degree (or higher) in Biochemistry, Molecular Biology, Chemistry, or related scientific field
  • Minimum 2–3 years’ experience in a regulated laboratory environment (GMP or similar)
  • Hands-on experience in analytical method development or validation for biologics
  • Familiarity with immunoassays (ELISA, nephelometry) and data analysis tools
  • Strong technical writing skills (SOPs, validation protocols, test reports)
  • Ability to work both independently and collaboratively in a project-driven setting
  • Proven organisational and time management skills
  • Must have full working rights in Australia

Health requirement
  • Audiometry
  • Set B – Informed consent consult, Hepatitis B antibodies only
  • Set A – Informed consent consult, HIV, Hepatitis C & Hepatitis B antibodies and Antigen
Culture
You’ll be joining a tight-knit team of six within a large, mission-driven organisation where scientific excellence, integrity, and collaboration are core values. The team encourages autonomy, proactive problem-solving, and mutual support, with access to world-class systems and technology.

Why this opportunity is right for you
This is a Full-time 12-month contract opportunity based in Melbourne working onsite Monday to Friday.

How to Apply
Click apply or contact Georgia, Senior Recruitment Consultant on +61370371653 for a confidential discussion.