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.