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.
Here’s What You’ll Do:- Request, sample and release raw materials in support of GMP manufacturing operations.
- Coordinate samples and collaborate cross-functionally with internal stakeholders and external laboratories.
- Train on and perform analytical and inspection methods, including HPLC, Bioanalyzer, osmolality, pH, appearance, conductivity, TruScan and dimensional verification.
- Inspect product and raw material retain samples.
- Perform sample logging and result entry in LabVantage LIMS, ensuring accurate and traceable laboratory records.
- Inspect and release raw materials and consumable components in accordance with approved specifications and procedures.
- Manage, maintain and troubleshoot controlled-temperature units to support compliant storage of laboratory materials and samples.
- Support facility environmental monitoring activities as required, including routine sampling within classified cleanroom environments.
- Manage and stock QC laboratory supplies and perform routine laboratory cleaning to maintain a safe, inspection-ready and compliant laboratory environment.
- Write and revise SOPs, protocols and reports.
- Complete and maintain cGMP documentation for all work performed, ensuring contemporaneous, accurate and compliant records.
- Participate in authoring quality system records, including deviations, change controls and CAPAs.
Here’s What You’ll Need (Basic Qualifications):- Education: Bachelor’s degree in a relevant scientific discipline.
- Experience: 2+ years of experience in a cGMP laboratory setting preferred.
Our client believes that an in-person culture is critical to their success. Therefore, this role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.
If this role sounds like something you'd be keen to discuss further, please reach out to me urgently at will.stewart@randstad.com.au. I will be conducting candidate interviews this week, intending to move forward to shortlist by the end of this week. At Randstad, we are passionate about providing equal employment opportunities and embracing diversity to the benefit of all. We actively encourage applications from any background.
