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.