GMP QC: Raw Materials Lab & Release – Melbourne

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 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.