qc - raw materials

HR Partners; Melbourne; On-site; AUD 55,000 - 83,000; Full time

Job summary

Randstad is supporting a global pharma/biotech client expanding in Melbourne. We are seeking a Quality Control Associate focused on Raw Materials, with GMP experience, for a contract role based in Clayton, offering Morning and Afternoon shifts.

In this hands-on position, you will sample, test, inspect and release raw materials within the QC laboratory, collaborating with internal teams and external laboratories to ensure compliance with cGMP and site requirements.

Qualifications

• Experience in GMP QC for raw materials.
• Experience in pharmaceutical QC laboratory environments.

Responsibilities

• Perform raw material sampling, testing, inspection and release.
• Collaborate with internal and external labs to ensure materials meet cGMP and site requirements.

Skills

Quality control

GMP experience

Job description

Randstad has been engaged to support one of our flagship clients, a global market leader in the pharma and biotech space. This company has a huge global outreach, and an emerging presence here in Australia. It's a very exciting time to be part of this operation as it continues its growth and increase in its operational capability here in Australia.We will be supporting them across a number of key vacancies within their Melbourne team.

Currently we are looking to speak with Quality Control Associates within Raw Materials, with expereince within GMP.

Shifts: Morning (6am – 2pm) and Afternoon (2pm - 10pm) available.

The Role:
Joining this client means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. This contract position is based at the client’s Clayton, Australia site and plays a hands-on role in supporting GMP manufacturing operations through raw material sampling, testing, inspection and release activities. Working as an individual contributor across the QC laboratory environment, you’ll collaborate closely with internal teams, external laboratories and other stakeholders to ensure materials, consumables and samples are managed in accordance with cGMP and site requirements.
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