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Analyst - QC Sample Management

Job description

Benefits
  • Work with one of the world’s most respected biopharma organisations
  • Suitable for graduate and early career scientists
  • Join a high-calibre scientific team working on impactful therapeutic products
  • Gain exposure to innovative QC sample management techniques
  • 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. With state-of-the-art laboratories, you’ll join a passionate team dedicated to maintaining the highest standards of quality, safety, and regulatory compliance.

About the role:
This role sits within the Quality Control function of a global biopharmaceutical manufacturer and is responsible for supporting cleanroom operations through environmental and utility sampling. The position involves gowning into graded cleanroom environments and following strict protocols to support product quality and regulatory compliance.

Responsibilities: 
  • Perform viable and non-viable environmental monitoring (air, surfaces, cleanroom areas)
  • Collect and manage samples of water, pure steam, and compressed gases
  • Accurately log and submit samples using LIMS systems
  • Gown and work within graded cleanroom environments (Grades A–D)
  • Follow GMP protocols and site SOPs for all sampling and handling activities
  • Support investigations into deviations or environmental monitoring issues
  • Communicate any sampling delays or issues that may impact timelines
  • Collaborate with team members to ensure consistent sampling coverage across site
Requirements: Best suited for recent graduates and early career scientists
  • Bachelor of Science e.g. Microbiology (MSc and above are overqualified)
  • Must have relevant working rights for 12 month contract role
  • Comfortable working in GMP-regulated environments
  • Clear written and verbal communication skills
  • Ability to follow structured procedures and work as part of a team-based QC function
  • Willingness to work in a physically active role, moving between manufacturing areas
Culture:
The team culture is structured, supportive, and compliance-focused, with a strong emphasis on teamwork, clear communication, and following procedures. It’s a hands-on role in a regulated environment where reliability, consistency, and accountability are highly valued.

Why this opportunity is right for you
This is a Full-time 12-month contract opportunity based in Melbourne

How to Apply
Click apply or contact Georgia, Senior Recruitment Consultant on ggraham@hpgconnect.com for a confidential discussion.

Health requirement
  • Flu Vaccination required
  • Audiometry
  • Ishihara colour vision screening