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GMP Science is seeking a Pharmaceutical Logistics Technician to manage inbound and outbound clinical trial medicines at a highly regulated 3PL depot. You will relabel, quality-check, and prepare cold-chain shipments for hospitals, research labs, and clinical sites.
Working within GMP procedures, you’ll store, label and release products while maintaining strict documentation and temperature controls across multiple environments. Training and on-call coverage are part of the role.
This is working with a major partner in the clinical trial, pharmaceutical, and medicine logistics industry. Operating from advanced, temperature-regulated facilities across Australia - and backed by a strong international presence, they provide vital storage and transport solutions for high-value medicines, vaccines, and GMP research-based products.
They work hand-in-hand with hospitals, clinics, universities and scientific institutions, ensuring essential medicines are held and delivered safely and reliably. With multiple industry accolades and a stellar reputation, this organisation is synonymous with quality, care, and innovation.
Despite their global scale, they’ve kept a people-first approach at their core. The team environment is supportive and down-to-earth, with a strong emphasis on it's people, growth and development. Many employees join for the mission and stay for the culture.
Position:
This Pharmaceutical Logistics Technician (internally called a Clinical Operations Tech) will be dealing with incoming and outgoing of clinical trial medicines at the highly regulated 3PL pharmaceutical depot and warehouse. You’ll be hands-on with relabelling, quality control, and cold-chain shipment prep for critical medicine moving across hospitals, research labs, and clinical sites.
You’ll be part of the ops team helping to ensure temperature-sensitive products are stored, labelled, and released correctly-following exact procedures and keeping everything compliant with GMP standards.
Duties include:
The benefits:
The experience you need:
You’ll ideally come from a pharmaceutical or science background, exposure to clinical trials is an advantage but not essential. Having knowledge of compliance, labelling, and exposure to industrial environments or depot/warehouse logistics is ideal. This is a detail-focused, hands-on role that suits someone reliable, accurate, and comfortable in fast-paced settings.
Summary of ideal background:
PR or Citizenship is needed due to security for this role.