QC - Raw Materials

Randstad Pty; Melbourne; On-site; AUD 70,000 - 100,000; Full time

Benefits offered by this job

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Job summary

Randstad Pty in Melbourne is supporting a flagship client in the pharma/biotech space. This contract role is based at the Clayton site, supporting GMP manufacturing operations with raw material sampling, testing, and release activities.

You will work as an individual contributor in a QC laboratory, collaborating with internal teams and external labs, ensuring compliant records and cGMP documentation across shifts.

Qualifications

• Bachelor’s degree in a relevant scientific discipline.
• 2+ years of experience in a cGMP laboratory setting preferred.

Responsibilities

• 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.
• 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.

Skills

HPLC

Bioanalyzer

Osmolality

pH measurement

Dimensional verification

Education

Bachelor's degree in a relevant scientific discipline

Tools

LabVantage LIMS

TruScan

Temperature-controlled storage

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.

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

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.

qualification

• 3-5 years previous experience preferred

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.