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Quality Control Analytical Technology Scientist

Healthcare Professionals Group
Broadmeadows, VIC
A$40-$43 p/h
Science & Technology → Biological & Biomedical Sciences
Contract
On-site

Posted 9 days ago


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.


About Healthcare Professionals Group

Melbourne, VIC, Australia

This company does not have any further information provided at this time. We encourage you to research the company by searching for them to learn more about the company or role in question before applying.

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