QA Officer

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

Job summary

Auspep, an Australian manufacturer of R&D and GMP chemicals, is seeking an experienced Quality Assurance Officer. You will ensure products released for distribution meet their intended purpose, and that the Quality system and processes comply with regulatory guidelines.

Reporting to the QA Manager, the role offers a supportive team in a flexible and inclusive workplace. Applicants with strong QA experience in pharma manufacturing will be valued.

Qualifications

• Tertiary qualifications in science, engineering or related field.
• Strong Quality experience in a manufacturing environment, preferably pharmaceuticals.
• 2+ years demonstrated experience in QA role. GMP experience is desirable.
• QC experience or knowledge of HPLC and other analytical testing would be advantageous.
• Validation experience would be desirable.

Responsibilities

• Reviewing batch manufacturing records and releasing raw materials, intermediates and final product.
• Preparing reports for deviations, OOSs and change controls.
• Preparing, reviewing and approving procedures, test methods and manufacturing records.
• Contributing to troubleshooting investigations and quality risk assessments.
• Participating in internal audit program.
• Providing training as required in Quality principles and GMP.

Skills

Quality assurance

GMP

Analytical testing

Technical writing

Education

Science/Engineering degree

Tools

HPLC

Microsoft Word

Microsoft Excel

Job description

Auspep is an Australian manufacturer of R&D and GMP chemicals for research, veterinary and therapeutics. We are now seeking for an experienced Quality Assurance Officer.

Your new role:

As QA Officer you will have a multi-faceted role in the organisation however your primary responsibility is to ensure that all products released for distribution are acceptable for their intentional purpose and that the Quality system and processes are maintained according to Regulatory guidelines.

Reporting to the QA Manager, this role will suit someone who is looking to make a genuine impact on the business whilst being part of a supportive team in a flexible and inclusive workplace.

What you will be doing:

• Reviewing batch manufacturing records and releasing raw materials, intermediates and final product
• Preparing reports for deviations, OOSs and change controls
• Preparing, reviewing and approving various documents such as procedures, test methods and manufacturing records
• Contributing to troubleshooting investigations and quality risk assessments
• Participating in internal audit program
• Providing training as required in Quality principles and GMP

What you will need to succeed:

• Tertiary qualifications in science, engineering or related field
• Strong Quality experience in a manufacturing environment, preferably pharmaceuticals
• 2+ years demonstrated experience in QA role. GMP experience is desirable
• QC experience or knowledge of HPLC and other analytical testing would be advantageous
• Validation experience would be desirable
• Ability to focus strongly on tasks and manage time effectively in a quality-focused manner
• Strong decision making and problem-solving skills
• Effective communication and interpersonal skills to successfully interact with colleagues, and ability to work effectively in a team environment
• Demonstrated attention to detail and an ability to think analytically
• Proficient skills in Microsoft platforms such as Word and Excel
• Advanced technical writing skills will be highly regarded

Applications close on 26 October 2026.

Only shortlisted candidates will be contacted.