About the role

Ceva Animal Health is seeking a technically capable and quality-focused QC Analyst to join our Quality Control team at our Glenorie manufacturing site.

Reporting to the QA/QC Manager, you will perform routine sampling and analytical testing of raw materials, in-process materials, finished products and other assigned samples. You will ensure testing and laboratory documentation are completed accurately, safely and in accordance with cGMP, GLP, APVMA requirements and Ceva’s Quality Management System.

This position would suit an experienced laboratory professional who is confident operating chromatography systems, troubleshooting analytical issues and working within a regulated environment.

Key responsibilities

• Perform routine sampling and testing of raw materials, in-process materials and finished products.
• Conduct physical, chemical and instrumental analysis using approved methods and specifications.
• Operate HPLC, UPLC and other laboratory instruments.
• Prepare samples, reagents, solutions, mobile phases and analytical standards.
• Review calculations, chromatographic data and analytical results for accuracy and completeness.
• Complete testing within required laboratory and production timelines.
• Identify and promptly escalate atypical, out-of-specification or out-of-trend results.
• Maintain accurate, contemporaneous and traceable laboratory records.
• Support laboratory investigations, deviations, CAPAs and change controls.
• Complete equipment checks, logbooks, calibration records and maintenance documentation.
• Assist with stability testing activities and program requirements.
• Contribute to test methods, SOPs, laboratory instructions and continuous-improvement initiatives.
• Maintain a safe, organised and inspection-ready laboratory environment.

About you

To be successful in this role, you will have:

• A degree in Chemistry, Pharmaceutical Science, Biochemistry or a related scientific field.
• Practical experience operating HPLC and/or UPLC systems.
• Strong knowledge of GxP requirements, particularly GLP and Good Documentation Practices.
• Demonstrated laboratory troubleshooting and problem-solving capability.
• Strong attention to detail and a commitment to accurate results and data integrity.
• The ability to follow detailed test methods, SOPs and safety procedures.
• Effective planning, organisation and time-management skills.
• The ability to work independently while contributing effectively within a team.

Experience in the following areas will be highly regarded:

• Waters LC instruments and Empower software.
• A GMP-regulated laboratory.
• Quality management systems, including deviations, CAPAs and change controls.
• Stability testing or stability program management.
• Pharmaceutical manufacturing, veterinary pharmaceuticals or another regulated industry.

Pre-employment requirements

The successful candidate will be required to complete a National Police Check as part of Ceva’s pre-employment screening process.

About Ceva

Ceva Animal Health is a global animal health company focused on developing innovative health solutions for animals. At our Glenorie site, you will work alongside experienced Quality, Manufacturing and Operations professionals in a collaborative and regulated environment.

If you are technically capable, quality-focused and comfortable working within a regulated QC laboratory, we would like to hear from you.