GMP Quality Control Analyst (Late Shift)

Moderna; Melbourne; Sur place; AUD 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Healthcare benefits

Well-being programs

Family-building benefits

Paid time off

Résumé du poste

Moderna seeks an analytical QC Scientist for its Melbourne facility. You will perform cGMP QC testing across chemistry, release, and stability areas, using HPLC/UPLC, UV, DLS, and plate readers. You will support stability programs, method transfers, and quality systems in a late-shift role.

The role requires a strong background in analytical chemistry, GMP experience, and collaboration with cross-functional teams to ensure data integrity and regulatory compliance.

Qualifications

• Bachelor's degree in a scientific discipline and GMP-regulated experience.
• Minimum 5 years' experience in a GMP pharmaceutical/biotech environment.
• Hands-on analytical chemistry with HPLC/UPLC, spectroscopy, particle analysis.
• Experience with quality systems and regulated labs.

Responsabilités

• Perform cGMP QC testing using HPLC/UPLC, UV, DLS, and plate readers.
• Support stability programs, method transfers, and qualification activities.
• Review and author GMP documentation, SOPs, and technical records.
• Assist investigations, deviations, CAPAs, and change controls.
• Coordinate with internal and regulatory inspections and audits.
• Drive continuous improvement to laboratory performance and compliance.

Connaissances

HPLC

UPLC

UV Spectroscopy

Dynamic Light Scattering

Plate reader assays

Formation

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or related

Outils

LIMS

Electronic quality systems

Description du poste

Moderna seeks an analytical QC Scientist for its Melbourne facility. You will perform cGMP QC testing across chemistry, release, and stability areas, using HPLC/UPLC, UV, DLS, and plate readers. You will support stability programs, method transfers, and quality systems in a late-shift role.

The role requires a strong background in analytical chemistry, GMP experience, and collaboration with cross-functional teams to ensure data integrity and regulatory compliance.