GMP QC Analyst — HPLC & Lab Validation

Bova Compounding; Sydney; On-site; AUD 85,000 - 110,000; Full time

Benefits offered by this job

Bova Anniversary Day

Team Bonding Events

Pet Carer’s Leave

Employee Assistance Program

Corporate Discounts

Job summary

Nextmune Laboratories, part of the Bova Aus group, is seeking a Full‑Time Quality Control Analyst to join the team. You will perform routine sampling, analytical testing and data interpretation to ensure compliant results in line with cGMP, GLP, APVMA requirements and the Quality Management System.

Reporting to the QA/QC Manager, you will operate HPLC/UPLC instruments, support method validation and stability studies, and contribute to ongoing improvements while maintaining safety and inspection

Qualifications

• Experience in HPLC analysis and method validation.
• GMP QC laboratory experience.
• Familiar with SOPs, audits and investigations.

Responsibilities

• Perform routine sampling and physical, chemical and instrumental testing of raw materials, in-process materials and finished products.
• Operate HPLC, UPLC and other laboratory instruments, including sample and reagent preparation.
• Review and interpret analytical data, calculations and results, ensuring accuracy and timely reporting.
• Support method validation, method transfer and stability studies, maintaining product quality data and analytical trends.
• Perform equipment checks, calibration, maintenance and troubleshooting, and assist with laboratory stock management.
• Identify and elevate OOS/OOT results and non-conformities, supporting investigations, deviations and CAPAs.
• Maintain accurate laboratory records and assist with reviewing and updating SOPs and laboratory procedures.
• Contribute to continuous improvement while maintaining a safe, organised and inspection-ready laboratory.

Skills

HPLC analysis

Analytical thinking

Attention to detail

Communication skills

Tools

HPLC

UPLC

SOPs

Job description

Nextmune Laboratories, part of the Bova Aus group, is seeking a Full‑Time Quality Control Analyst to join the team. You will perform routine sampling, analytical testing and data interpretation to ensure compliant results in line with cGMP, GLP, APVMA requirements and the Quality Management System.

Reporting to the QA/QC Manager, you will operate HPLC/UPLC instruments, support method validation and stability studies, and contribute to ongoing improvements while maintaining safety and inspection